Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.94411066G>ACA257800COL1A2c.1262G>A (p.Gly421Asp)
c.1256G>A (p.Gly419Asp)
 ClinVar dbSNP
7g.94411066G=CA1726754815COL1A2c.1262G= (p.Gly421=)
c.1256G= (p.Gly419=)
 dbSNP

Number of alleles fetched