Allele Registry

Canonical Allele Identifier: PA2825756887

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000518215

RCV001239622

RCV001834664

RCV003144306

ClinVar Variation:

447285

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124452.1:p.Arg1063Cys	CA1706459 NM_001130980.2:c.3187C>T