Allele Registry

Canonical Allele Identifier: PA658806906

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 500922

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124459.1:p.Cys1379Arg	CA1706900 NM_001130987.2:c.4135T>C