Allele Registry

Canonical Allele Identifier: PA2825760035

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV001141005

RCV003145356

ClinVar Variation:

897608

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124453.1:p.Glu1871Lys	CA1707448 NM_001130981.2:c.5611G>A