Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.121846919A>CCA115059HPDc.774T>G (p.Tyr258Ter)
c.657T>G (p.Tyr219Ter)
 ClinVar dbSNP
12g.121846919A=CA2068077955HPDc.774T= (p.Tyr258=)
c.657T= (p.Tyr219=)
 dbSNP

Number of alleles fetched