Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.94410260G>ACA16618574COL1A2c.1054G>A (p.Gly352Ser)
c.1048G>A (p.Gly350Ser)
ClinVar dbSNP
7g.94410260G=CA1726752773COL1A2c.1054G= (p.Gly352=)
c.1048G= (p.Gly350=)
dbSNP

Number of alleles fetched