Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.102877503G>ACA229534PAHc.400C>T (p.Gln134Ter)
c.385C>T (p.Gln129Ter)
n.496C>T
c.384C>T
n.489C>T
 ClinVar dbSNP
12g.102877503G=CA2059462480PAHc.400C= (p.Gln134=)
c.385C= (p.Gln129=)
n.496C=
c.384C=
n.489C=
 dbSNP

Number of alleles fetched