Canonical Allele Identifier: PA2828915284
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 949378
ClinVar RCV Id: RCV001220826

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369637.1:p.Leu469Pro
CA350699256
NM_001382708.1:c.1406T>C