Allele Registry

Canonical Allele Identifier: PA2825747690

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000262612

RCV000725415

RCV000763505

RCV000791498

RCV003401245

RCV003469231

ClinVar Variation:

284254

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124448.1:p.Arg945Trp	CA1706331 NM_001130976.2:c.2833C>T