Allele Registry

Canonical Allele Identifier: PA2825613121

Gene: TP53 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

363560

ClinVar RCV:

RCV000422077

RCV000422980

RCV000424901

RCV000427034

RCV000427749

RCV000430410

RCV000431652

RCV000432320

RCV000433236

RCV000437254

RCV000437968

RCV000439980

RCV000440667

RCV000442863

RCV000443687

RCV000443828

RCV000704312

RCV002356520

RCV004022251

ClinVar Variation:

376681

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001119588.1:p.Tyr73Cys	CA16603095 NM_001126116.1:c.218A>G