Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.189001554G>ACA005350COL3A1c.2257G>A (p.Gly753Arg)
c.2356G>A (p.Gly786Arg)
 ClinVar dbSNP
2g.189001554G=CA1315401924COL3A1c.2257G= (p.Gly753=)
c.2356G= (p.Gly786=)
 dbSNP

Number of alleles fetched