RS199474720 TPM3
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What This Variant Does
"Mutations of the slow muscle alpha-tropomyosin gene, TPM3, are a rare cause of nemaline myopathy. Mu...
Associated Conditions
Congenital myopathy 4B
autosomal recessive
Congenital myopathy with fiber type disproportion
Congenital myopathy 4B
autosomal recessive
Congenital myopathy with fiber type disproportion
Other Variants in TPM3