Allele Registry

Canonical Allele Identifier: PA100375

Gene: DES HGNC NCBI

ClinVar RCV:

RCV000056781

RCV000627795

RCV001787806

RCV001798009

ClinVar Variation:

16826

HGVS (amino-acid)	Matching Registered Transcripts
NP_001918.3:p.Arg406Trp	CA257646 NM_001927.4:c.1216C>T