Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.188997211G>TCA004553COL3A1c.1709G>T (p.Gly570Val)
c.1808G>T (p.Gly603Val)
 ClinVar dbSNP
2g.188997211G>ACA004546COL3A1c.1709G>A (p.Gly570Asp)
c.1808G>A (p.Gly603Asp)
 ClinVar dbSNP

Number of alleles fetched