Allele Registry

Canonical Allele Identifier: PA217089

Gene: DES HGNC NCBI

ClinVar RCV:

RCV000056812

ClinVar Variation:

66421

HGVS (amino-acid)	Matching Registered Transcripts
NP_001918.3:p.Leu274Pro	CA217087 NM_001927.4:c.821T>C