Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.108591178G>ACA258453COL4A5c.1286G>A (p.Gly429Glu)
n.742G>A
c.962G>A (p.Gly321Glu)
c.1301G>A (p.Gly434Glu)
c.-424G>A (n.-424G>A)
ClinVar dbSNP
Xg.108591178G=CA2450686432COL4A5c.1286G= (p.Gly429=)
n.742G=
c.962G= (p.Gly321=)
c.1301G= (p.Gly434=)
c.-424G= (n.-424G=)
dbSNP

Number of alleles fetched