Allele Registry

Canonical Allele Identifier: PA2825764659

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 194354

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124456.1:p.Leu449Pro	CA240279 NM_001130984.2:c.1346T>C