Allele Registry

Canonical Allele Identifier: PA2826565607

Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376670

ClinVar RCV Id: RCV000417716 RCV000420083 RCV000422099 RCV000427972 RCV000426649 RCV000428855 RCV000431215 RCV000437749 RCV000439081 RCV000437980 RCV000442710 RCV000785309 RCV001042741 RCV002365461 RCV003321589 RCV004022246

ClinVar Variation Id: 406596

ClinVar RCV Id: RCV000466409 RCV001270272

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263689.1:p.Val177Leu	CA16603084 NM_001276760.3:c.529G>T CA16615950 NM_001276760.3:c.529G>C