Allele Registry

Canonical Allele Identifier: PA2579935191

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score -0.1977225999

Score -0.443294066

Score 1.6001516941

Score 0.432773425

Score 0.3885061419

Score 0.249940666

Linked Data - NCBI & NCI

ClinVar Allele:

363478

ClinVar RCV:

RCV000418385

RCV000419449

RCV000422508

RCV000427774

RCV000427875

RCV000429067

RCV000430162

RCV000436692

RCV000437360

RCV000437805

RCV000438569

RCV000439724

RCV000443459

RCV000538079

RCV001270273

RCV001567979

RCV002379286

ClinVar Variation:

376599

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Gly244Cys	CA16603021 NM_000546.6:c.730G>T