Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.108580721G>CCA258341COL4A5c.874G>C (p.Gly292Arg)
c.550G>C (p.Gly184Arg)
c.889G>C (p.Gly297Arg)
ClinVar dbSNP
Xg.108580721G>ACA413926389COL4A5c.874G>A (p.Gly292Arg)
c.550G>A (p.Gly184Arg)
c.889G>A (p.Gly297Arg)
ClinVar dbSNP
Xg.108580721G=CA2450683098COL4A5c.874G= (p.Gly292=)
c.550G= (p.Gly184=)
c.889G= (p.Gly297=)
dbSNP

Number of alleles fetched