Gene table: search width pubmed_id = 7663526


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Disease phenotype
Item
in
this
table
Key
references
Gene symbol (chromosome)

protein
All allelic disease phenotypes - locus/disease symbols
Congenital myopathy 4A, dominant - (AD)
3.4
1347195
7663526
TPM3 (1q21.2)
Tropomyosin 3
* Nemaline myopathy 1, autosomal dominant - NEM1