Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.94947919T>GCA119594CYP2C9c.622T>G (p.Leu208Val)
n.393T>G
ClinVar dbSNP
10g.94947919T=CA1929296794CYP2C9c.622T= (p.Leu208=)
n.393T=
dbSNP

Number of alleles fetched