Allele Registry

Canonical Allele Identifier: PA2828917388

Gene: DES HGNC NCBI

ClinVar RCV:

RCV001367750

RCV001762638

ClinVar Variation:

1058593

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369642.1:p.Arg325Gly	CA350695130 NM_001382713.1:c.973C>G