Canonical Allele Identifier: PA2828915314
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 2440744

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369638.1:p.Ala21Thr
CA2125009
NM_001382709.1:c.61G>A