Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.110186513C>TCA343271COL4A1c.1769G>A (p.Gly590Glu)
n.1899G>A
c.1577G>A (p.Gly526Glu)
 ClinVar dbSNP
13g.110186513C=CA2118738833COL4A1c.1769G= (p.Gly590=)
n.1899G=
c.1577G= (p.Gly526=)
 dbSNP

Number of alleles fetched