Allele Registry

Canonical Allele Identifier: PA2825768501

Gene: DYSF HGNC NCBI

ClinVar Variation Id: 538646

HGVS (amino-acid)	Matching Registered Transcripts
NP_001124457.1:p.Arg1949Cys	CA1707548 NM_001130985.2:c.5845C>T