Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.102840483G>TCA229409PAHc.1232C>A (p.Ser411Ter)
c.1217C>A (p.Ser406Ter)
n.894C>A
c.336C>A
n.747C>A
c.1175C>A (p.Ser392Ter)
ClinVar dbSNP
12g.102840483G=CA2059441893PAHc.1232C= (p.Ser411=)
c.1217C= (p.Ser406=)
n.894C=
c.336C=
n.747C=
c.1175C= (p.Ser392=)
dbSNP
12g.102840483G>CCA16020974PAHc.1232C>G (p.Ser411Ter)
c.1217C>G (p.Ser406Ter)
n.894C>G
c.336C>G
n.747C>G
c.1175C>G (p.Ser392Ter)
ClinVar dbSNP

Number of alleles fetched