Allele Registry

Canonical Allele Identifier: PA2829466903

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 497494

HGVS (amino-acid)	Matching Registered Transcripts
NP_003485.1:p.Arg847Trp	CA1706231 NM_003494.4:c.2539C>T