Allele Registry

Canonical Allele Identifier: PA1139683910

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV001244959

RCV001835219

ClinVar Variation:

969577

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124459.1:p.Arg236Gly	CA1705422 NM_001130987.2:c.706C>G