Allele Registry

Canonical Allele Identifier: PA110796

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000262612

RCV000725415

RCV000763505

RCV000791498

RCV003401245

RCV003469231

ClinVar Variation:

284254

HGVS (amino-acid)	Matching Registered Transcripts
NP_003485.1:p.Arg959Trp	CA1706331 NM_003494.4:c.2875C>T