Allele Registry

Canonical Allele Identifier: PA2825601386

Gene: TP53 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000417655

RCV000417883

RCV000418371

RCV000425994

RCV000427865

RCV000430718

RCV000436003

RCV000436185

RCV000438999

RCV000785257

RCV001362325

RCV002418243

ClinVar Variation:

376596

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001119584.1:p.Phe270Ile	CA16603018 NM_001126112.3:c.808T>A