Canonical Allele Identifier: PA2828917051
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 1339289

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369642.1:p.Arg10Cys
CA350682181
NM_001382713.1:c.28C>T