Allele Registry

Canonical Allele Identifier: PA100340

Gene: DES HGNC NCBI

ClinVar RCV:

RCV000056769

RCV000239682

ClinVar Variation:

66390

HGVS (amino-acid)	Matching Registered Transcripts
NP_001918.3:p.Ala357Pro	CA217007 NM_001927.4:c.1069G>C