Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.94425163G>ACA257750COL1A2c.2720G>A (p.Gly907Asp)
n.503G>A
n.2693G>A
c.2714G>A (p.Gly905Asp)
 ClinVar dbSNP
7g.94425163G=CA1726780778COL1A2c.2720G= (p.Gly907=)
n.503G=
n.2693G=
c.2714G= (p.Gly905=)
 dbSNP

Number of alleles fetched