Allele Registry

Canonical Allele Identifier: PA2828914831

Gene: DES HGNC NCBI

ClinVar RCV:

RCV001867087

ClinVar Variation:

1355754

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369637.1:p.Arg16Ser	CA350682339 NM_001382708.1:c.46C>A