Canonical Allele Identifier: PA2828915219
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 1481128

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369637.1:p.Ala396Ser
CA350694898
NM_001382708.1:c.1186G>T