Canonical Allele Identifier: PA2828916950
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 2925199

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369641.1:p.Asn366Ser
CA350694194
NM_001382712.1:c.1097A>G