Allele Registry

Canonical Allele Identifier: PA100419

Gene: DES HGNC NCBI

ClinVar RCV:

RCV000056779

RCV002265588

ClinVar Variation:

66396

HGVS (amino-acid)	Matching Registered Transcripts
NP_001918.3:p.Asp399Tyr	CA217032 NM_001927.4:c.1195G>T