Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.102855150G>ACA229695PAHc.692C>T (p.Ser231Phe)
c.677C>T (p.Ser226Phe)
n.788C>T
 ClinVar dbSNP
12g.102855150G=CA2059449089PAHc.692C= (p.Ser231=)
c.677C= (p.Ser226=)
n.788C=
 dbSNP

Number of alleles fetched