ClinGen Allele Registry
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Chr
Mutation (hg38)
CAid
Gene
Transcript
Linkouts
X
g.9743637G>T
CA226190
GPR143
c.695C>A (p.Thr232Lys)
c.443C>A (p.Thr148Lys)
ClinVar
dbSNP
gnomAD v4
X
g.9743637G>A
CA10344958
GPR143
c.695C>T (p.Thr232Met)
c.443C>T (p.Thr148Met)
ClinVar
dbSNP
ExAC
gnomAD v2
gnomAD v3
gnomAD v4
COSMIC
Number of alleles fetched
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