Canonical Allele Identifier: PA2828917368
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 1481128

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369642.1:p.Ala307Ser
CA350694898
NM_001382713.1:c.919G>T