Allele Registry

Canonical Allele Identifier: PA2825762504

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 538642

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124455.1:p.Glu542Gly	CA1705883 NM_001130983.2:c.1625A>G