Allele Registry

Canonical Allele Identifier: PA2825759578

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 288624

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124453.1:p.Arg1440Cys	CA1706966 NM_001130981.2:c.4318C>T