Allele Registry

Canonical Allele Identifier: PA2829467928

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 288624

HGVS (amino-acid)	Matching Registered Transcripts
NP_003485.1:p.Arg1423Cys	CA1706966 NM_003494.4:c.4267C>T