Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.21178691C>ACA384105660SLCO1B1c.597C>A (p.Phe199Leu)
dbSNP
12g.21178691C>TCA6476742SLCO1B1c.597C>T (p.Phe199=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.21178691C=CA2020991484SLCO1B1c.597C= (p.Phe199=)
dbSNP

Number of alleles fetched