Allele Registry

Canonical Allele Identifier: PA2828916936

Gene: DES HGNC NCBI

ClinVar RCV:

RCV001225519

ClinVar Variation:

953258

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369641.1:p.Arg350Leu	CA350693836 NM_001382712.1:c.1049G>T