Allele Registry

Canonical Allele Identifier: PA2826561531

Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376595

ClinVar RCV Id: RCV000423824 RCV000426634 RCV000426445 RCV000432152 RCV000433231 RCV000434093 RCV000438906 RCV000442796 RCV000443660

ClinVar Variation Id: 634778

ClinVar RCV Id: RCV000785520 RCV001321223 RCV002422673 RCV004027353 RCV003492171

ClinVar Variation Id: 1431729

ClinVar RCV Id: RCV001940898 RCV004042022

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263625.1:p.Phe231Leu	CA16603017 NM_001276696.3:c.693T>G CA397837037 NM_001276696.3:c.693T>A CA397837052 NM_001276696.3:c.691T>C