Allele Registry

Canonical Allele Identifier: PA2829467329

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 497848

HGVS (amino-acid)	Matching Registered Transcripts
NP_003485.1:p.Arg1084Cys	CA1706513 NM_003494.4:c.3250C>T