Gene table: search width pubmed_id = 18572189


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

protein
All allelic disease phenotypes - locus/disease symbols
Familial hypertrophic cardiomyopathy, 13 - (AD)
10.12
18572189
TNNC1 (3p21.3-p14.3)
Slow troponin C
* Cardiomyopathy, dilated, 1Z - CMD1Z
* Familial hypertrophic cardiomyopathy, 13 - CMH13