Allele Registry

Canonical Allele Identifier: PA2829465983

Gene: DYSF HGNC NCBI

ClinVar RCV:

RCV001244959

RCV001835219

ClinVar Variation:

969577

HGVS (amino-acid)	Matching Registered Transcripts
NP_003485.1:p.Arg204Gly	CA1705422 NM_003494.4:c.610C>G