Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.50196670C>GCA400222713COL1A1c.805G>C (p.Gly269Arg)
n.532G>C
 ClinVar dbSNP
17g.50196670C>TCA260326COL1A1c.805G>A (p.Gly269Ser)
n.532G>A
 ClinVar dbSNP

Number of alleles fetched