Canonical Allele Identifier: PA2828916308
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 1310579

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369640.1:p.Gln165Arg
CA350686649
NM_001382711.1:c.494A>G