RS104893748 MYL3
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What This Variant Does
"Mutations in either the essential or regulatory light chains of myosin are associated with a rare my...
Associated Conditions
Hypertrophic cardiomyopathy 8
Hypertrophic cardiomyopathy
Cardiovascular phenotype
Hypertrophic cardiomyopathy 8
Hypertrophic cardiomyopathy
Cardiovascular phenotype
Other Variants in MYL3