Allele Registry

Canonical Allele Identifier: PA2825765267

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV003738749

ClinVar Variation:

2912979

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124456.1:p.Arg1025Pro	CA347217058 NM_001130984.2:c.3074G>C