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ell
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ines
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Mutations and CNAs (1)
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PHGDH
Mutation
Missense
ENST00000369409.4
g.120284468C>T
g.120284468C>T
c.1157C>T
c.1157C>T
p.Ala386Val
p.Ala386Val
benign
benign
JHH2
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