Allele Registry

Canonical Allele Identifier: PA2825755115

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 94324

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124451.1:p.Lys1511Thr	CA222170 NM_001130979.2:c.4532A>C