Allele Registry

Canonical Allele Identifier: PA658811710

Gene: DES HGNC NCBI

ClinVar RCV:

RCV000591625

RCV001046462

RCV002456300

RCV002491191

ClinVar Variation:

498618

HGVS (amino-acid)	Matching Registered Transcripts
NP_001918.3:p.Thr77Ala	CA2125045 NM_001927.4:c.229A>G