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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
3
g.52451399T>C
CA297331
TNNC1
c.446A>G (p.Asp149Gly)
ClinVar
dbSNP
3
g.52451399T=
CA1364863618
TNNC1
c.446A= (p.Asp149=)
dbSNP
Number of alleles fetched
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