Allele Registry

Canonical Allele Identifier: PA308268

Gene: DES HGNC NCBI

ClinVar RCV:

RCV000183350

RCV001337313

ClinVar Variation:

201704

HGVS (amino-acid)	Matching Registered Transcripts
NP_001918.3:p.Trp295Gly	CA308266 NM_001927.4:c.883T>G