Allele Registry

Canonical Allele Identifier: PA2826563025

Gene: TP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 376668

ClinVar RCV Id: RCV000417683 RCV000421780 RCV000423312 RCV000427345 RCV000427493 RCV000428483 RCV000429213 RCV000432458 RCV000434691 RCV000433209 RCV000438383 RCV000440549 RCV000439916 RCV000442009 RCV000443390 RCV000694763 RCV000785539 RCV001821147 RCV002289542 RCV002289541

ClinVar Variation Id: 2185665

ClinVar RCV Id: RCV002596262 RCV004069069

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001263627.1:p.Val14Leu	CA16603082 NM_001276698.3:c.40G>T CA397841537 NM_001276698.3:c.40G>C