Allele Registry

Canonical Allele Identifier: PA2825760174

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000596899

ClinVar Variation:

501582

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124453.1:p.Cys2009Arg	CA347226529 NM_001130981.2:c.6025T>C