Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.108625732G>TCA258794COL4A5c.3044G>T (p.Gly1015Val)
n.2500G>T
c.277G>T
c.2720G>T (p.Gly907Val)
c.617G>T (p.Gly206Val)
c.3059G>T (p.Gly1020Val)
c.1379G>T (p.Gly460Val)
dbSNP
Xg.108625732G=CA2450697896COL4A5c.3044G= (p.Gly1015=)
n.2500G=
c.277G=
c.2720G= (p.Gly907=)
c.617G= (p.Gly206=)
c.3059G= (p.Gly1020=)
c.1379G= (p.Gly460=)
dbSNP

Number of alleles fetched