Allele Registry

Canonical Allele Identifier: PA2829467755

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000266196

RCV000343174

RCV000392904

RCV001140152

RCV003380540

ClinVar Variation:

290670

HGVS (amino-acid)	Matching Registered Transcripts
NP_003485.1:p.Arg1342Gln	CA1706890 NM_003494.4:c.4025G>A