Allele Registry

Canonical Allele Identifier: PA2825751387

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 501816

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124450.1:p.Glu157Lys	CA1705382 NM_001130978.2:c.469G>A