Canonical Allele Identifier: PA2828916035
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 1481128

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369639.1:p.Ala374Ser
CA350694898
NM_001382710.1:c.1120G>T