Allele Registry

Canonical Allele Identifier: PA2829466132

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 287822

HGVS (amino-acid)	Matching Registered Transcripts
NP_003485.1:p.Ala315Thr	CA1705596 NM_003494.4:c.943G>A