Gene table: search width pubmed_id = 31070086


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

protein
All allelic disease phenotypes - locus/disease symbols
Congenital amyotrophy - (AR)
5.50
31070086
CACNA1H (16p13.3)
Calcium channel, voltage-dependent, T type, aplpha-1H subunit
* Congenital amyotrophy