Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.108577953G>ACA258289COL4A5c.611G>A (p.Gly204Asp)
c.287G>A (p.Gly96Asp)
c.626G>A (p.Gly209Asp)
 ClinVar dbSNP
Xg.108577953G>TCA258292COL4A5c.611G>T (p.Gly204Val)
c.287G>T (p.Gly96Val)
c.626G>T (p.Gly209Val)
 dbSNP

Number of alleles fetched