The association between CALM2 (Calmodulin 2) and Long Qt Syndrome 1 is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording likely-pathogenic variants and a causative germline mutation.
Sources3
Clinical variants135
Symptoms18
Compounds0
Trials0
Publications15
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.