Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.188990308G>ACA007350COL3A1c.746G>A (p.Gly249Asp)
ClinVar dbSNP COSMIC COSMIC
2g.188990308G>TCA007357COL3A1c.746G>T (p.Gly249Val)
ClinVar dbSNP

Number of alleles fetched