Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.108578087G>ACA258308COL4A5c.655G>A (p.Gly219Ser)
c.331G>A (p.Gly111Ser)
c.670G>A (p.Gly224Ser)
 ClinVar dbSNP
Xg.108578087G=CA2450682222COL4A5c.655G= (p.Gly219=)
c.331G= (p.Gly111=)
c.670G= (p.Gly224=)
 dbSNP

Number of alleles fetched