Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.108581019G>ACA258359COL4A5c.928G>A (p.Gly310Arg)
c.604G>A (p.Gly202Arg)
c.943G>A (p.Gly315Arg)
 ClinVar dbSNP
Xg.108581019G=CA2450683200COL4A5c.928G= (p.Gly310=)
c.604G= (p.Gly202=)
c.943G= (p.Gly315=)
 dbSNP

Number of alleles fetched