Allele Registry

Canonical Allele Identifier: PA2828917322

Gene: DES HGNC NCBI

ClinVar RCV:

RCV001225519

ClinVar Variation:

953258

HGVS (amino-acid)	Matching Registered Transcripts
NP_001369642.1:p.Arg260Leu	CA350693836 NM_001382713.1:c.779G>T