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Finnish Disease Heritage
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Diseases
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GCSH
Glycine cleavage system H protein
Ensembl gene entry
Ensembl gene location
Omim gene
Genetics Home Reference entry
Diseases associated to this gene:
NKH
Finnish Mutations
Mutation
Consequence
Amino acid change
Reference sequence
Articles
Foreign Mutations
Mutation
Consequence
Amino acid change
Reference sequence
Population
Articles
IVS4-1G>T
Japanese
12402263
Koyata-1
Japanese
1671321
Koyata-2
Japanese
1671321
Koyata-3
Japanese
1671321