Allele Registry

Canonical Allele Identifier: PA658806685

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 538630

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124459.1:p.Arg419Gln	CA1705662 NM_001130987.2:c.1256G>A