Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.189001398G>ACA005290COL3A1c.2186G>A (p.Gly729Asp)
c.2285G>A (p.Gly762Asp)
 ClinVar dbSNP
2g.189001398G>TCA005297COL3A1c.2186G>T (p.Gly729Val)
c.2285G>T (p.Gly762Val)
 ClinVar dbSNP

Number of alleles fetched