Allele Registry

Canonical Allele Identifier: PA2829466639

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 283484

HGVS (amino-acid)	Matching Registered Transcripts
NP_003485.1:p.Gly653Ser	CA1706026 NM_003494.4:c.1957G>A