Allele Registry

Canonical Allele Identifier: PA2579952074

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.4415136062

Score -0.7274564273

Score -0.1774096291

Linked Data - NCBI & NCI

ClinVar Allele:

469117

ClinVar RCV:

RCV000527123

RCV000561902

RCV000664300

RCV000986056

RCV000989706

RCV003330753

ClinVar Variation:

458574

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Arg306Gln	CA287486566 NM_000546.6:c.917G>A