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Mutations on the Protein: P09417 From Positions: 24 To 37

2
1
0
1



Swiss-Prot Disease: VAR_006961
p.TRP36ARG
N/A
N/A
Hyperphenylalaninemia, BH4-deficient, C (HPABH4C)


OMIM Disease: 612676.0004
p.TRP36ARG
N/A
N/A
HYPERPHENYLALANINEMIA, BH4-DEFICIENT, C






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