Allele Registry

Canonical Allele Identifier: PA2825748679

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 283243

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124448.1:p.Cys1801Phe	CA10604436 NM_001130976.2:c.5402G>T