Canonical Allele Identifier: PA2828917334
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 2925199

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369642.1:p.Asn276Ser
CA350694194
NM_001382713.1:c.827A>G