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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
X
g.78123292A>T
CA120831
PGK1
c.854A>T (p.Asp285Val)
c.770A>T (p.Asp257Val)
n.261A>T
ClinVar
dbSNP
X
g.78123292A=
CA2439140516
PGK1
c.854A= (p.Asp285=)
c.770A= (p.Asp257=)
n.261A=
dbSNP
Number of alleles fetched
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