Allele Registry

Canonical Allele Identifier: PA2579952748

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.414390845

Score -0.21363988

Score 0.645253776

Score 0.295475788

Score 0.340071652

Score 0.416853394

Score 0.039060551

Score 0.01807212

Score -0.995591688

Score 0.460131513

Score -0.077486002

Score -0.303195232

Score 0.402997748

Score 0.414032245

Score -0.271809315

Score 0.686715987

Score 0.270641376

Score -0.634379403

Score 0.6559342426

Score 0.6675579156

Score 0.542016636

Score 0.837505509

Score 0.85112062

Score 0.653545172

Score -0.06745176

Score 0.206338112

Score -0.153778009

Score -0.767337272

Score 0.486945669

Score 0.590690566

Score 0.295889421

Score 0.52559828

Score -1.4488781236

Score 0.281745601

Score -0.082730752

Score 0.151627016

Score 0.241948154

Score -0.309529522

Score 0.756397975

Score 0.416641134

Score -0.377473767

Score -0.274417373

Score -0.688992909

Linked Data - NCBI & NCI

ClinVar Allele:

363531

ClinVar RCV:

RCV000417693

RCV000418362

RCV000420498

RCV000422668

RCV000423297

RCV000424776

RCV000425100

RCV000425394

RCV000425782

RCV000427544

RCV000427948

RCV000430735

RCV000432207

RCV000432931

RCV000433611

RCV000435050

RCV000435353

RCV000436038

RCV000437882

RCV000440334

RCV000441010

RCV000441711

RCV000444356

RCV000444427

RCV000444519

RCV000626118

RCV000633396

RCV001026425

RCV004022238

ClinVar Variation:

376652

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Arg248Gly	CA16603069 NM_000546.6:c.742C>G