Allele Registry

Canonical Allele Identifier: PA2579935878

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -1.2237701765

Score 1.5866390662

Score 1.2419360775

Score 0.135244427

Linked Data - NCBI & NCI

ClinVar Allele:

420659

ClinVar RCV:

RCV000492442

RCV000702915

RCV004023278

ClinVar Variation:

428866

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.His168Arg	CA287488569 NM_000546.6:c.503A>G