Allele Registry

Canonical Allele Identifier: PA658674798

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 471324

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124459.1:p.Arg2083Trp	CA1707654 NM_001130987.2:c.6247C>T