Allele Registry

Canonical Allele Identifier: PA2829468471

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 471314

HGVS (amino-acid)	Matching Registered Transcripts
NP_003485.1:p.Arg1677Cys	CA1707255 NM_003494.4:c.5029C>T