Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.189002316G>ACA005368COL3A1c.2311G>A (p.Gly771Ser)
c.2410G>A (p.Gly804Ser)
 ClinVar dbSNP
2g.189002316G=CA1315402254COL3A1c.2311G= (p.Gly771=)
c.2410G= (p.Gly804=)
 dbSNP

Number of alleles fetched