Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.73418269delCA170815ALBc.1610del (p.Ile537AsnfsTer21)
c.1265del (p.Ile422AsnfsTer21)
c.1034del (p.Ile345AsnfsTer21)
c.*889del (n.*889del)
n.264del
c.1160del (p.Ile387AsnfsTer21)
n.1157del
c.1143del
c.971del (p.Ile324AsnfsTer21)
ClinVar dbSNP
4g.73418269T=CA1468146972ALBc.1610T= (p.Ile537=)
c.1265T= (p.Ile422=)
c.1034T= (p.Ile345=)
c.*889T= (n.*889T=)
n.264T=
c.1160T= (p.Ile387=)
n.1157T=
c.1143T=
c.971T= (p.Ile324=)
dbSNP dbSNP

Number of alleles fetched