Allele Registry

Canonical Allele Identifier: PA2579936016

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 1.7437000529

Score -0.012355223

Score -0.9171318607

Score 0.6102893828

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000417784

RCV000417996

RCV000422633

RCV000423257

RCV000425147

RCV000426543

RCV000427160

RCV000432450

RCV000433975

RCV000434565

RCV000434994

RCV000437830

RCV000439618

RCV000442522

RCV000445223

RCV000785535

RCV001023834

RCV003621529

RCV004022204

ClinVar Variation:

376571

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Cys176Gly	CA16602997 NM_000546.6:c.526T>G