Allele Registry

Canonical Allele Identifier: PA169158

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -2.110460535

Score 0.0415607433

Score 0.762345938

Score -0.9811042494

Score -3.244998051

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000013182

RCV000132058

RCV000144671

RCV000536677

RCV001030736

RCV001192620

RCV003476892

ClinVar Variation:

12382

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Ala189Val	CA000270 NM_000546.6:c.566C>T