Allele Registry

Canonical Allele Identifier: PA2825765269

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000351237

RCV000665378

RCV001297834

RCV003469226

ClinVar Variation:

282449

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124456.1:p.Arg1026Trp	CA1706450 NM_001130984.2:c.3076C>T