Allele Registry

Canonical Allele Identifier: PA915973677

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV000523223

RCV001829489

RCV002527605

RCV004023559

ClinVar Variation:

450192

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124454.1:p.Arg851Trp	CA1706191 NM_001130982.2:c.2551C>T