ClinGen Allele Registry
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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
12
g.71938935A>G
CA10642412
TPH2
c.-52A>G (n.-52A>G)
n.49A>G
ClinVar
dbSNP
gnomAD v2
gnomAD v3
gnomAD v4
12
g.71938935A>C
CA2045506653
TPH2
c.-52A>C (n.-52A>C)
n.49A>C
dbSNP
Number of alleles fetched
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