Allele Registry

Canonical Allele Identifier: PA2579934285

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -0.047660208

Score -1.7477991762

Score 2.0969220628

Score 1.0862269887

Score 0.078950759

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000417926

RCV000419216

RCV000420739

RCV000422309

RCV000426460

RCV000427997

RCV000430547

RCV000433017

RCV000437350

RCV000437992

RCV000438674

RCV000439356

RCV000441270

RCV000567850

RCV000688854

RCV000785477

RCV001584114

RCV004022235

ClinVar Variation:

376645

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Pro278Ala	CA16603062 NM_000546.6:c.832C>G