Allele Registry

Canonical Allele Identifier: PA106738

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -1.5832722132

Score 0.295776247

Score 0.634311445

Score -0.738275095

Score 0.333230564

Score 0.762520127

Score 0.669596017

Score 0.388078994

Score 0.623965497

Score -0.045963607

Score 0.402986354

Score 0.611912753

Score 0.341753643

Score 1.7951773645

Score 0.458417534

Score 0.24105089

Score 0.359575984

Score -0.132951383

Score 0.031651904

Score 0.341974639

Score -0.363388682

Score -0.117305053

Score 0.50556303

Score 0.377175451

Score 0.590095036

Score -0.866596857

Score 0.371254108

Score 0.172172738

Score 0.457875451

Score -0.767337272

Score 0.384505387

Score 0.161679608

Score 0.926372755

Score 0.036005272

Score 0.720513298

Score 0.385709617

Score 0.785828062

Score 0.036019693

Score 0.484891152

Score 0.703121576

Score 0.460371873

Score 0.23818791

Score 0.325432508

Score 1.266317784

Score 0.230363586

Score 0.685198957

Score 0.522354976

Score 0.468013739

Score 0.042961218

Linked Data - NCBI & NCI

ClinVar Allele:

622586

ClinVar RCV:

RCV000785275

RCV000814073

RCV001027249

RCV002290030

RCV002487616

ClinVar Variation:

634682

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Arg273Gly	CA397836977 NM_000546.6:c.817C>G