Allele Registry

Canonical Allele Identifier: PA915974113

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000812166

RCV001089590

RCV001830775

RCV003461204

ClinVar Variation:

655896

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124454.1:p.Glu1367Lys	CA1706854 NM_001130982.2:c.4099G>A