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MYL3

Official Full Name
myosin light chain 3
Organism
Homo sapiens
GeneID
4634
Background
MYL3 encodes myosin light chain 3, an alkali light chain also referred to in the literature as both the ventricular isoform and the slow skeletal muscle isoform. Mutations in MYL3 have been identified as a cause of mid-left ventricular chamber type hypertrophic cardiomyopathy. [provided by RefSeq, Jul 2008]
Synonyms
CMH8; VLC1; VLCl; MLC1V; MLC1SB; MLC-lV/sb;

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