Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.134805044C>TCA281098COL5A1c.3184C>T (p.Arg1062Ter)
n.3586C>T
n.3582C>T
 ClinVar dbSNP COSMIC
9g.134805044C=CA1883381225COL5A1c.3184C= (p.Arg1062=)
n.3586C=
n.3582C=
 dbSNP

Number of alleles fetched