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Search Results: 1 unique variant retrieved.
c.626C>T
p.Thr209Ile (163)
Mutation Type:
Polymorphism
Domain:
Act-Peptide
Nucleotide number:
20468
Mutation Effect:
Missense
Location:
Exon(6)
CpG:
-
No. of patients reported:
1
No. of bases:
1
Structural Information
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