Allele Registry

Canonical Allele Identifier: PA162472

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -0.2703708788

Score 0.3078599049

Score -0.524369381

Linked Data - NCBI & NCI

ClinVar Allele:

133284

ClinVar RCV:

RCV000115742

RCV000122173

RCV000123100

RCV000409871

RCV000586196

RCV001030741

RCV003492490

RCV003945046

ClinVar Variation:

127827

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Val31Ile	CA357868 NM_000546.6:c.91G>A