Allele Registry

Canonical Allele Identifier: PA2825608094

Gene: TP53 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000421427

RCV000423188

RCV000427039

RCV000427702

RCV000431675

RCV000433885

RCV000437948

RCV000440391

RCV000442701

RCV000444957

RCV000445284

RCV002298583

ClinVar Variation:

376616

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001119586.1:p.His214Leu	CA16603036 NM_001126114.3:c.641A>T