Allele Registry

Canonical Allele Identifier: PA2826561157

Gene: TP53 HGNC NCBI

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_001263625.1:p.Tyr166Asp	CA16603100 NM_001276696.3:c.496T>G