Allele Registry

Canonical Allele Identifier: PA100467

Gene: DES HGNC NCBI

ClinVar RCV:

RCV000056765

RCV001044194

ClinVar Variation:

16825

HGVS (amino-acid)	Matching Registered Transcripts
NP_001918.3:p.Leu345Pro	CA217003 NM_001927.4:c.1034T>C