Allele Registry

Canonical Allele Identifier: PA2579935412

Gene: TP53 HGNC NCBI

Linked Data - Variant Effect Evidence

MaveDb:

Score 0.173005171

Score 0.555608337

Score -1.1364105712

Score 0.418381531

Score 1.7288241602

Score 1.4582450005

Linked Data - NCBI & NCI

ClinVar Allele:

363565

ClinVar RCV:

RCV000419128

RCV000421137

RCV000421350

RCV000423676

RCV000426948

RCV000428535

RCV000428939

RCV000430021

RCV000434351

RCV000434446

RCV000436740

RCV000438356

RCV000439629

RCV000439865

RCV000444122

RCV000444873

RCV000462351

RCV000663307

RCV003441853

ClinVar Variation:

376686

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_000537.3:p.Tyr205Asp	CA16603100 NM_000546.6:c.613T>G