Allele Registry

Canonical Allele Identifier: PA2579936234

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -2.975039707

Score -0.2245681489

Score 0.1662439815

Score 0.3886643451

Linked Data - NCBI & NCI

ClinVar Allele:

479274

ClinVar RCV:

RCV000569500

RCV001056511

RCV002289830

ClinVar Variation:

485032

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Asp148Ala	CA287488644 NM_000546.6:c.443A>C