Allele Registry

Canonical Allele Identifier: PA915974233

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 288624

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124454.1:p.Arg1455Cys	CA1706966 NM_001130982.2:c.4363C>T