Allele Registry

Canonical Allele Identifier: PA166357

Gene: TP53 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

151478

ClinVar RCV:

RCV000130398

RCV000413074

RCV000538977

RCV000763416

RCV001255676

RCV002247507

RCV002288637

RCV003149899

RCV003460927

ClinVar Variation:

141764

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001119586.1:p.Arg267Trp	CA000423 NM_001126114.3:c.799C>T