Allele Registry

Canonical Allele Identifier: PA2579952481

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -1.3357500518

Score 0.115722922

Score 0.239255744

Score 0.547920966

Score 0.435368374

Score 0.34792885

Score 0.468343237

Score 0.157372905

Score 0.25947078

Score 0.646406024

Score 0.352018569

Score -0.08708183

Score -0.342341012

Score 0.241590434

Score 0.037713904

Score 0.500022324

Score -0.474601615

Score 0.2794529

Score 0.199403033

Score 0.391533295

Score 0.079646361

Score 0.815027425

Score 0.775086618

Score 0.895407549

Score 0.640154725

Score 0.819202312

Score 0.453495945

Score 0.182896947

Score 0.780222445

Score 0.832604708

Score 0.966357359

Score 0.314970926

Score 0.347398381

Score 0.740135263

Score -0.075923034

Score 0.801392464

Score -0.204178431

Score 0.26551025

Score 1.5537579568

Score 0.299735472

Score 0.241948154

Score 0.092324992

Score 0.011670464

Score 0.248054499

Score 1.3034190855

Score 0.406721296

Score 0.327345562

Score 0.730835737

Score 0.450013489

Score 0.419883076

Score 0.059797962

Linked Data - NCBI & NCI

ClinVar Allele:

236461

ClinVar RCV:

RCV000222860

RCV000418732

RCV000419080

RCV000419328

RCV000419898

RCV000420123

RCV000421059

RCV000422030

RCV000426561

RCV000426712

RCV000427328

RCV000427811

RCV000429434

RCV000429654

RCV000431744

RCV000431835

RCV000434099

RCV000436356

RCV000437116

RCV000437377

RCV000439039

RCV000439246

RCV000440313

RCV000442511

RCV000444938

RCV000553607

RCV000785460

RCV002288863

ClinVar Variation:

231060

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Arg273Pro	CA10580917 NM_000546.6:c.818G>C