Allele Registry

Canonical Allele Identifier: PA2826561570

Gene: TP53 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000419235

RCV000419912

RCV000420599

RCV000423341

RCV000423990

RCV000425744

RCV000426441

RCV000430590

RCV000431286

RCV000434260

RCV000436480

RCV000437115

RCV000438476

RCV000441019

RCV000441335

RCV000441960

RCV000580293

RCV001234533

RCV002521506

ClinVar Variation:

376583

960924

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263625.1:p.Cys236Ser	CA16603007 NM_001276696.3:c.707G>C CA397836943 NM_001276696.3:c.706T>A