Allele Registry

Canonical Allele Identifier: PA106729

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.3143042398

Score -0.148212672

Score 0.183275859

Score 0.852644299

Score 0.423506769

Score -0.062257019

Score 0.290224038

Score 0.238636383

Score 0.529727785

Score 0.518935174

Score 1.2613472537

Score 0.139977712

Score -0.202019323

Score -0.887343916

Score -0.129667493

Score 0.128800975

Score 0.078480057

Score 0.034058372

Score -0.255739334

Score -0.930398222

Score -0.144152645

Score 0.597105824

Score -0.247222254

Score -0.274417373

Score -0.010954139

Score -0.125418529

Score 0.408314801

Score -0.734007858

Score 0.40872222

Score -0.317947477

Score 0.346692197

Score 0.261702151

Score 0.493021571

Score 0.468943407

Score 0.292721598

Score -0.455832579

Score 0.320152593

Score 0.108773728

Score 0.271682947

Score 0.145623148

Score 0.336806614

Score 0.876398123

Score 0.056757552

Score 0.566117631

Score 0.382446946

Score 0.540419826

Score 0.369541714

Score 0.125108029

Linked Data - NCBI & NCI

ClinVar Allele:

52763

ClinVar RCV:

RCV000131966

RCV000144665

RCV000149051

RCV000205625

RCV000254692

RCV000421090

RCV000431786

RCV000432002

RCV000442470

RCV000785470

RCV003466889

ClinVar Variation:

43594

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Arg273Cys	CA000432 NM_000546.6:c.817C>T