Allele Registry

Canonical Allele Identifier: PA2579934209

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -0.204714395

Score 0.2218163794

Score -0.1230843548

Score 0.150391943

Score 0.433800351

Score -0.5580871826

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000417671

RCV000419836

RCV000420516

RCV000422083

RCV000422714

RCV000424389

RCV000424902

RCV000430093

RCV000430695

RCV000431703

RCV000432322

RCV000432958

RCV000438151

RCV000439711

RCV000440370

RCV000440974

RCV000443165

RCV000443254

RCV000470818

RCV000499361

RCV000633352

RCV000658764

RCV000785286

RCV000785325

RCV002446643

RCV002446795

ClinVar Variation:

376587

406568

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Asp281Glu	CA10590135 NM_000546.6:c.843C>G CA16615937 NM_000546.6:c.843C>A