Allele Registry

Canonical Allele Identifier: PA2825755048

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 288624

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124451.1:p.Arg1454Cys	CA1706966 NM_001130979.2:c.4360C>T