Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.189006207G>ACA005988COL3A1c.2942G>A (p.Gly981Glu)
c.3041G>A (p.Gly1014Glu)
c.2528-1847G>A (n.2528-1847G>A)
 ClinVar dbSNP COSMIC
2g.189006207G=CA1315404019COL3A1c.2942G= (p.Gly981=)
c.3041G= (p.Gly1014=)
c.2528-1847G= (n.2528-1847G=)
 dbSNP

Number of alleles fetched