Allele Registry

Canonical Allele Identifier: PA2825748172

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 500922

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124448.1:p.Cys1347Arg	CA1706900 NM_001130976.2:c.4039T>C