Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.108578078G>ACA258301COL4A5c.646G>A (p.Gly216Arg)
c.322G>A (p.Gly108Arg)
c.661G>A (p.Gly221Arg)
 ClinVar dbSNP
Xg.108578078G=CA2450682217COL4A5c.646G= (p.Gly216=)
c.322G= (p.Gly108=)
c.661G= (p.Gly221=)
 dbSNP

Number of alleles fetched