Allele Registry

Canonical Allele Identifier: PA658674640

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 450303

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124459.1:p.Arg1169Cys	CA1706610 NM_001130987.2:c.3505C>T