Allele Registry

Canonical Allele Identifier: PA300265

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.2870366223

Score 0.18586264

Score -3.111615223

Score -2.068907443

Score -2.998007588

Score -3.504522049

Score -1.873577953

Score -0.180981652

Score 0.435918228

Score 0.143403316

Score 0.14529632

Score -1.75813797

Score 0.0789377

Score 0.5666055807

Score -1.260689678

Score 0.511396847

Score 0.499489974

Score -4.721517956

Score 0.267798727

Score 0.011670464

Score -2.539887996

Score -0.4737834403

Score 0.28027837

Score 0.297674915

Score 0.450813717

Score -2.913348607

Score -2.393647686

Score -0.363388682

Score -0.455832579

Score -2.05537453

Score -1.06758038

Score -4.138008811

Score -0.153778009

Score -2.09500949

Score 0.47729692

Score -1.804277098

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000161038

RCV000213059

RCV000633381

RCV001527101

RCV003150958

RCV003467273

ClinVar Variation:

182938

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Arg282Leu	CA000456 NM_000546.6:c.845G>T