Allele Registry

Canonical Allele Identifier: PA2825762089

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 501816

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124455.1:p.Glu158Lys	CA1705382 NM_001130983.2:c.472G>A