The association between MYL2 (Myosin Light Chain 2) and Cardiomyopathy, Familial Hypertrophic, 10 is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, pathogenic and likely-pathogenic variants, and causative variation.
Sources4
Clinical variants404
Symptoms33
Compounds0
Trials0
Publications38
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.