Allele Registry

Canonical Allele Identifier: PA107215

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -1.4729136384

Score 1.3558851909

Score 0.595651834

Score 0.169596281

Score 1.4555745661

Linked Data - NCBI & NCI

ClinVar Allele:

363521

ClinVar RCV:

RCV000421997

RCV000426679

RCV000427094

RCV000427714

RCV000432228

RCV000432977

RCV000433428

RCV000435645

RCV000437941

RCV000439725

RCV000442821

RCV000443572

RCV000444293

RCV000522600

RCV000562528

RCV000633344

RCV000785527

RCV004022233

ClinVar Variation:

376642

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Pro278Ser	CA16603059 NM_000546.6:c.832C>T