Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.110170583C>TCA341444COL4A1c.3706G>A (p.Gly1236Arg)
c.3514G>A (p.Gly1172Arg)
 ClinVar dbSNP
13g.110170583C=CA2118734117COL4A1c.3706G= (p.Gly1236=)
c.3514G= (p.Gly1172=)
 dbSNP

Number of alleles fetched