Allele Registry

Canonical Allele Identifier: PA107000

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.727349698

Score 0.022533304

Score 0.699898345

Score 0.674315204

Score 0.402566612

Score 0.0442444678

Score 0.5042743148

Score 0.094864114

Score 0.54015164

Score 0.256855066

Score 0.283115757

Score 1.2177588867

Score 0.305538795

Score 0.31556904

Score 0.245800279

Score 0.014828377

Score -2.39488862

Score 0.431365102

Score 0.037301511

Score 0.343361759

Score 0.297868724

Score 0.419465637

Score 0.218821291

Score 0.47916075

Score 0.717667826

Linked Data - NCBI & NCI

ClinVar Allele:

27388

ClinVar RCV:

RCV000013142

RCV000161025

RCV000417593

RCV000418673

RCV000419737

RCV000423577

RCV000424262

RCV000425471

RCV000426090

RCV000428895

RCV000430002

RCV000434535

RCV000436186

RCV000436330

RCV000440197

RCV000440886

RCV000441334

RCV000443435

RCV000492412

RCV000633397

RCV001271056

ClinVar Variation:

12349

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Gly245Cys	CA000369 NM_000546.6:c.733G>T