Gene table: search width pubmed_id = 14676148


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

protein
All allelic disease phenotypes - locus/disease symbols
Short QT syndrome 1 - (AD)
10.153
14676148
KCNH2 (7q36.1)
Voltage-gated potassium channel, subfamily H, member 2
* Short qt syndrome 1 - SQT1
* Long QT syndrome-2 - LQT2