Canonical Allele Identifier: PA2828917002
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 1058593

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369641.1:p.Arg415Gly
CA350695130
NM_001382712.1:c.1243C>G