Allele Registry

Canonical Allele Identifier: PA2825765357

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 287474

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124456.1:p.Arg1084Cys	CA1706529 NM_001130984.2:c.3250C>T