Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.189001425G>ACA16610666COL3A1c.2213G>A (p.Gly738Asp)
c.2312G>A (p.Gly771Asp)
 ClinVar dbSNP
2g.189001425G=CA1315401858COL3A1c.2213G= (p.Gly738=)
c.2312G= (p.Gly771=)
 dbSNP

Number of alleles fetched