Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.108578319G>ACA258318COL4A5c.716G>A (p.Gly239Glu)
c.392G>A (p.Gly131Glu)
c.731G>A (p.Gly244Glu)
 ClinVar dbSNP
Xg.108578319G=CA2450682323COL4A5c.716G= (p.Gly239=)
c.392G= (p.Gly131=)
c.731G= (p.Gly244=)
 dbSNP

Number of alleles fetched