Allele Registry

Canonical Allele Identifier: PA2579955258

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -0.5194013819

Score -0.3024828135

Score -0.4813541852

Linked Data - NCBI & NCI

ClinVar Allele:

242993

ClinVar RCV:

RCV000226793

RCV001021387

RCV002288916

RCV003469151

ClinVar Variation:

237949

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Pro13Leu	CA10583685 NM_000546.6:c.38C>T