Allele Registry

Canonical Allele Identifier: PA2825757018

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 450303

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124452.1:p.Arg1168Cys	CA1706610 NM_001130980.2:c.3502C>T