Allele Registry

Canonical Allele Identifier: PA2825770169

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000358891

RCV001140902

RCV001833383

ClinVar Variation:

288624

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124458.1:p.Arg1410Cys	CA1706966 NM_001130986.2:c.4228C>T