Allele Registry

Canonical Allele Identifier: PA2826561938

Gene: TP53 HGNC NCBI

Linked Data

ClinVar RCV:

RCV000417695

RCV000417973

RCV000420789

RCV000421853

RCV000423292

RCV000426502

RCV000427175

RCV000428674

RCV000429260

RCV000432550

RCV000433227

RCV000433943

RCV000437826

RCV000438042

RCV000438407

RCV000439947

RCV000440632

RCV000443785

RCV000445268

RCV000529132

RCV000785555

RCV001023983

RCV001591055

RCV003983035

RCV004022216

ClinVar Variation:

376606

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263626.1:p.His20Arg	CA16603027 NM_001276697.3:c.59A>G