Allele Registry

Canonical Allele Identifier: PA100395

Gene: DES HGNC NCBI

ClinVar RCV:

RCV000056799

RCV001384253

ClinVar Variation:

66411

HGVS (amino-acid)	Matching Registered Transcripts
NP_001918.3:p.Asn116Ser	CA217067 NM_001927.4:c.347A>G