Allele Registry

Canonical Allele Identifier: PA2825758098

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 284469

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124453.1:p.Val69Gly	CA10604804 NM_001130981.2:c.206T>G