Allele Registry

Canonical Allele Identifier: PA106758

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.117889556

Score -0.30958761

Score 0.946919183

Score -0.079463162

Score -0.083503949

Score -0.256304929

Score -0.362085134

Score 0.30313262

Score 0.525077546

Score -0.8912211369

Score -0.022891135

Score 0.503532144

Score 0.310070677

Score -0.22488892

Score 0.50822428

Score 0.857951233

Score 0.045985443

Score 0.381220176

Score 0.397829487

Score 0.291417769

Score -0.377473767

Score 0.449465342

Score 0.058889555

Score -0.116443804

Score 0.442425508

Score -0.503137896

Score 0.14187466

Score -0.091155289

Score 0.664437706

Score -0.441915861

Score 0.538965426

Score 0.393414919

Score 0.201610338

Score -0.385997046

Score -0.362572888

Score 0.445117881

Score 0.257367454

Score 0.179207894

Score 0.902238501

Score 1.3460604052

Score 0.123217297

Score 0.682632422

Score 0.667612602

Score 0.144665273

Score 0.044502842

Score 0.373299385

Score 0.14529632

Score 0.186970618

Score 0.21675501

Score 0.431744988

Score -0.032816807

Linked Data - NCBI & NCI

ClinVar Allele:

363534

ClinVar RCV:

RCV000418536

RCV000418738

RCV000421259

RCV000423490

RCV000423633

RCV000423981

RCV000425890

RCV000426132

RCV000427314

RCV000428692

RCV000429444

RCV000431067

RCV000433315

RCV000434296

RCV000434695

RCV000435767

RCV000436818

RCV000437048

RCV000438507

RCV000441792

RCV000442241

RCV000444109

RCV000444782

RCV000444989

RCV000515526

RCV000568814

RCV000785524

RCV000822080

RCV001539823

RCV002289534

RCV002502455

ClinVar Variation:

376655

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Arg273Leu	CA001530 NM_000546.6:c.818G>T