Allele Registry

Canonical Allele Identifier: PA2579934611

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 1.1393935406

Score 0.596946051

Score 1.757456323

Score 0.512391998

Score -1.4187081663

Score 0.074235168

Score 0.023865026

Score -0.194194184

Score 1.306407262

Score -0.389159645

Linked Data - NCBI & NCI

ClinVar Allele:

363483

ClinVar RCV:

RCV000418277

RCV000419444

RCV000420527

RCV000424643

RCV000425790

RCV000426804

RCV000429713

RCV000430767

RCV000431462

RCV000432081

RCV000436041

RCV000437043

RCV000439119

RCV000441708

RCV000444043

RCV000444128

RCV000633351

RCV001026295

RCV004022215

ClinVar Variation:

376604

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Gly245Arg	CA16603025 NM_000546.6:c.733G>C