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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
16
g.29813701C>G
CA317033
PRRT2
c.647C>G (p.Pro216Arg)
ClinVar
dbSNP
ExAC
gnomAD
16
g.29813701C>T
CA285795
PRRT2
c.647C>T (p.Pro216Leu)
ClinVar
dbSNP
ExAC
gnomAD
16
g.29813701C>A
CA317031
PRRT2
c.647C>A (p.Pro216His)
ClinVar
dbSNP
ExAC
gnomAD
Number of alleles fetched
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