Allele Registry

Canonical Allele Identifier: PA2579936914

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -0.366033457

Score 1.6836661899

Score -1.0911563887

Score 1.0056250534

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000421931

RCV000424730

RCV000433045

RCV000433598

RCV000434970

RCV000442091

RCV000442462

RCV000443054

RCV001041362

RCV004022228

ClinVar Variation:

376632

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Leu111Gln	CA16603051 NM_000546.6:c.332T>A