Allele Registry

Canonical Allele Identifier: PA2579935785

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.191071316

Score 2.1823175823

Score 0.9634202421

Score -1.7603406936

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000418455

RCV000419153

RCV000421182

RCV000421399

RCV000424145

RCV000426044

RCV000429147

RCV000429875

RCV000430527

RCV000432060

RCV000432754

RCV000437220

RCV000441241

RCV000441421

RCV000442290

RCV000445056

RCV000807434

RCV003463825

ClinVar Variation:

376016

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Val173Gly	CA16602485 NM_000546.6:c.518T>G