Allele Registry

Canonical Allele Identifier: PA2825747951

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 450303

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124448.1:p.Arg1137Cys	CA1706610 NM_001130976.2:c.3409C>T