Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.110187311C>TCA341456COL4A1c.1555G>A (p.Gly519Arg)
n.1685G>A
c.1363G>A (p.Gly455Arg)
 ClinVar dbSNP
13g.110187311C=CA2118741273COL4A1c.1555G= (p.Gly519=)
n.1685G=
c.1363G= (p.Gly455=)
 dbSNP

Number of alleles fetched