Canonical Allele Identifier: PA2828916336
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 2099541

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369640.1:p.Asp185Val
CA350687089
NM_001382711.1:c.554A>T