Allele Registry

Canonical Allele Identifier: PA2828916526

Gene: DES HGNC NCBI

ClinVar RCV:

RCV001367750

RCV001762638

ClinVar Variation:

1058593

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369640.1:p.Arg408Gly	CA350695130 NM_001382711.1:c.1222C>G