Allele Registry

Canonical Allele Identifier: PA2825754696

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 287474

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124451.1:p.Arg1128Cys	CA1706529 NM_001130979.2:c.3382C>T