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Finnish Disease Heritage
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C10orf2
CHROMOSOME 10 OPEN READING FRAME 2
Ensembl gene entry
Ensembl gene location
Omim gene
Genetics Home Reference entry
Diseases associated to this gene:
IOSCA
Finnish Mutations
Mutation
Consequence
Amino acid change
Reference sequence
Articles
c.1708A>G
Y508C
AF292004
16135556
Foreign Mutations
Mutation
Consequence
Amino acid change
Reference sequence
Population
Articles