Allele Registry

Canonical Allele Identifier: PA2825755400

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 538624

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124451.1:p.Arg1780His	CA1707346 NM_001130979.2:c.5339G>A