Allele Registry

Canonical Allele Identifier: PA645477741

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 94324

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124459.1:p.Lys1519Thr	CA222170 NM_001130987.2:c.4556A>C