Allele Registry

Canonical Allele Identifier: PA2825766637

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 499205

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124457.1:p.Pro249Leu	CA1705435 NM_001130985.2:c.746C>T