Allele Registry

Canonical Allele Identifier: PA645477549

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 287822

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124459.1:p.Ala347Thr	CA1705596 NM_001130987.2:c.1039G>A