Allele Registry

Canonical Allele Identifier: PA2825747415

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 283228

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124448.1:p.Ala684Val	CA1706065 NM_001130976.2:c.2051C>T