Allele Registry

Canonical Allele Identifier: PA2829467458

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 450303

HGVS (amino-acid)	Matching Registered Transcripts
NP_003485.1:p.Arg1151Cys	CA1706610 NM_003494.4:c.3451C>T