Allele Registry

Canonical Allele Identifier: PA2825758247

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV001244959

RCV001835219

ClinVar Variation:

969577

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124453.1:p.Arg235Gly	CA1705422 NM_001130981.2:c.703C>G