Allele Registry

Canonical Allele Identifier: PA2826563599

Gene: TP53 HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

363557

ClinVar RCV:

RCV000418040

RCV000420871

RCV000422166

RCV000422877

RCV000428087

RCV000428696

RCV000429377

RCV000433566

RCV000435261

RCV000439367

RCV000440106

RCV000701251

ClinVar Variation:

376678

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263627.1:p.Val115Leu	CA16603092 NM_001276698.3:c.343G>C