Allele Registry

Canonical Allele Identifier: PA2825766969

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 538642

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124457.1:p.Glu559Gly	CA1705883 NM_001130985.2:c.1676A>G