Allele Registry

Canonical Allele Identifier: PA168337

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.4032659933

Score -2.0586325

Score 0.426762309

Score -0.3527253218

Linked Data - NCBI & NCI

ClinVar Allele:

152145

ClinVar RCV:

RCV000131548

RCV000458425

RCV000679368

RCV001030738

RCV001527096

RCV003467176

ClinVar Variation:

142431

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Gly108Ser	CA000114 NM_000546.6:c.322G>A