Allele Registry

Canonical Allele Identifier: PA2825759852

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 471314

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124453.1:p.Arg1715Cys	CA1707255 NM_001130981.2:c.5143C>T