Allele Registry

Canonical Allele Identifier: PA2825766305

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000596899

ClinVar Variation:

501582

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124456.1:p.Cys1979Arg	CA347226529 NM_001130984.2:c.5935T>C