Allele Registry

Canonical Allele Identifier: PA658806645

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 501816

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124459.1:p.Glu189Lys	CA1705382 NM_001130987.2:c.565G>A