Allele Registry

Canonical Allele Identifier: PA2579951116

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.6692203472

Score -0.8847934664

Score -0.541562095

Linked Data - NCBI & NCI

ClinVar Allele:

236441

ClinVar RCV:

RCV000213880

RCV000541338

RCV001537143

RCV002288853

ClinVar Variation:

230306

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Gly360Glu	CA10580905 NM_000546.6:c.1079G>A