Allele Registry

Canonical Allele Identifier: PA2579934378

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.249865534

Score -0.3021979676

Score 1.1079042295

Score 0.3176241722

Score 0.408481022

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000220597

RCV000417840

RCV000422392

RCV000422798

RCV000423426

RCV000424659

RCV000427379

RCV000428065

RCV000429134

RCV000433685

RCV000434748

RCV000434911

RCV000435298

RCV000437591

RCV000439374

RCV000440058

RCV000444283

RCV000444359

RCV000445304

RCV001854689

RCV002288888

ClinVar Variation:

233303

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Gly266Val	CA10580919 NM_000546.6:c.797G>T