Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.127818341G>ACA16606222ENGc.919C>T (p.Gln307Ter)
c.1465C>T (p.Gln489Ter)
n.1408G>A
ClinVar dbSNP
9g.127818341G=CA1879986300ENGc.919C= (p.Gln307=)
c.1465C= (p.Gln489=)
n.1408G=
dbSNP

Number of alleles fetched