Allele Registry

Canonical Allele Identifier: PA2825692750

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 284469

HGVS (amino-acid)	Matching Registered Transcripts
NP_001123927.1:p.Val70Gly	CA10604804 NM_001130455.2:c.209T>G