Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.188999569G>ACA005209COL3A1c.2122G>A (p.Gly708Ser)
c.2221G>A (p.Gly741Ser)
 ClinVar dbSNP COSMIC COSMIC
2g.188999569G>TCA349840969COL3A1c.2122G>T (p.Gly708Cys)
c.2221G>T (p.Gly741Cys)
 ClinVar dbSNP

Number of alleles fetched