Allele Registry

Canonical Allele Identifier: PA2829468820

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 283243

HGVS (amino-acid)	Matching Registered Transcripts
NP_003485.1:p.Cys1815Phe	CA10604436 NM_003494.4:c.5444G>T