Allele Registry

Canonical Allele Identifier: PA2579935206

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.754118718

Score -1.2653662148

Score 1.8065147603

Score -0.113927129

Score 0.025611621

Score 0.313501662

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000421176

RCV000422301

RCV000426248

RCV000427088

RCV000431852

RCV000432981

RCV000438025

RCV000439518

RCV000443891

RCV000444573

RCV000444665

RCV000463978

RCV000566931

RCV002289545

ClinVar Variation:

376694

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Tyr236Asn	CA16040589 NM_000546.6:c.706T>A