Allele Registry

Canonical Allele Identifier: PA2825756332

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 538642

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124452.1:p.Glu558Gly	CA1705883 NM_001130980.2:c.1673A>G