Allele Registry

Canonical Allele Identifier: PA2829468781

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000725163

RCV001085921

RCV001276862

RCV003939934

RCV004021072

ClinVar Variation:

281104

HGVS (amino-acid)	Matching Registered Transcripts
NP_003485.1:p.Arg1796Trp	CA1707403 NM_003494.4:c.5386C>T