Allele Registry

Canonical Allele Identifier: PA106882

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.196324789

Score -0.9227563641

Score 1.2689323911

Score 0.513493244

Score -0.44985493

Score 1.5832589668

Linked Data - NCBI & NCI

ClinVar Allele:

363456

ClinVar RCV:

RCV000417486

RCV000420677

RCV000422044

RCV000422283

RCV000423396

RCV000427246

RCV000428630

RCV000428804

RCV000430919

RCV000433478

RCV000435170

RCV000437321

RCV000437476

RCV000438876

RCV000439946

RCV000443356

RCV000444792

RCV000785550

RCV001390630

RCV002365460

ClinVar Variation:

376577

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Cys238Gly	CA16603003 NM_000546.6:c.712T>G