Canonical Allele Identifier: PA2828915459
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 1311914

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369638.1:p.Glu139Gln
CA2125066
NM_001382709.1:c.415G>C