Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.108595557G>ACA258482COL4A5c.1472G>A (p.Gly491Glu)
n.928G>A
c.1148G>A (p.Gly383Glu)
c.1487G>A (p.Gly496Glu)
c.-194G>A (n.-194G>A)
dbSNP COSMIC
Xg.108595557G=CA2450687744COL4A5c.1472G= (p.Gly491=)
n.928G=
c.1148G= (p.Gly383=)
c.1487G= (p.Gly496=)
c.-194G= (n.-194G=)
dbSNP

Number of alleles fetched