Allele Registry

Canonical Allele Identifier: PA2825750943

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 283243

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124449.1:p.Cys1822Phe	CA10604436 NM_001130977.2:c.5465G>T