Allele Registry

Canonical Allele Identifier: PA2825749526

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 538642

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124449.1:p.Glu527Gly	CA1705883 NM_001130977.2:c.1580A>G