Canonical Allele Identifier: PA2828916003
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 2925199

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369639.1:p.Asn343Ser
CA350694194
NM_001382710.1:c.1028A>G