Allele Registry

Canonical Allele Identifier: PA2829465912

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 501816

HGVS (amino-acid)	Matching Registered Transcripts
NP_003485.1:p.Glu157Lys	CA1705382 NM_003494.4:c.469G>A