Allele Registry

Canonical Allele Identifier: PA2825764728

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 538642

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124456.1:p.Glu528Gly	CA1705883 NM_001130984.2:c.1583A>G