Allele Registry

Canonical Allele Identifier: PA2825759851

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 471315

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124453.1:p.Arg1715His	CA1707257 NM_001130981.2:c.5144G>A