Allele Registry

Canonical Allele Identifier: PA110869

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000812166

RCV001089590

RCV001830775

RCV003461204

ClinVar Variation:

655896

HGVS (amino-acid)	Matching Registered Transcripts
NP_003485.1:p.Glu1335Lys	CA1706854 NM_003494.4:c.4003G>A