Gene table: search width pubmed_id = 19487656


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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 4B, recessive - (AR)
3.5
19487656
19553118
TPM3 (1q21.2)
Tropomyosin 3
* Nemaline myopathy 1, autosomal dominant - NEM1