Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.94404867G>ACA16605302COL1A2c.407G>A (p.Gly136Asp)
c.401G>A (p.Gly134Asp)
ClinVar dbSNP COSMIC
7g.94404867G=CA1726792263COL1A2c.407G= (p.Gly136=)
c.401G= (p.Gly134=)
dbSNP

Number of alleles fetched