Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.87566218C>ACA123373ABCB1c.554G>T (p.Gly185Val)
c.362G>T (p.Gly121Val)
c.764G>T (p.Gly255Val)
ClinVar dbSNP COSMIC
7g.87566218C=CA1723648216ABCB1c.554G= (p.Gly185=)
c.362G= (p.Gly121=)
c.764G= (p.Gly255=)
dbSNP
7g.87566218C>GCA368090600ABCB1c.554G>C (p.Gly185Ala)
c.362G>C (p.Gly121Ala)
c.764G>C (p.Gly255Ala)
dbSNP

Number of alleles fetched