The association between TRPC3 (Transient Receptor Potential Cation Channel Subfamily C Member 3) and Spinocerebellar Ataxia 41 is well established and manually curated, with its 5 contributing sources — 4 of them expert-curated — recording a known molecular basis, pathogenic variants, and a causative germline mutation.
Sources5
Clinical variants8
Symptoms9
Compounds0
Trials0
Publications1
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.