Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.50197767C>ACA127139COL1A1c.661G>T (p.Gly221Cys)
n.388G>T
 ClinVar dbSNP
17g.50197767C>TCA400224750COL1A1c.661G>A (p.Gly221Ser)
n.388G>A
 ClinVar dbSNP COSMIC

Number of alleles fetched