Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.188996171G>ACA004390COL3A1c.1556G>A (p.Gly519Glu)
c.1655G>A (p.Gly552Glu)
 ClinVar dbSNP COSMIC COSMIC
2g.188996171G=CA1315399298COL3A1c.1556G= (p.Gly519=)
c.1655G= (p.Gly552=)
 dbSNP

Number of alleles fetched