Allele Registry

Canonical Allele Identifier: PA2825765612

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000812166

RCV001089590

RCV001830775

RCV003461204

ClinVar Variation:

655896

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124456.1:p.Glu1322Lys	CA1706854 NM_001130984.2:c.3964G>A