Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.102852911A>TCA229740PAHc.746T>A (p.Leu249His)
c.731T>A (p.Leu244His)
n.505T>A
 ClinVar dbSNP
12g.102852911A=CA2059446571PAHc.746T= (p.Leu249=)
c.731T= (p.Leu244=)
n.505T=
 dbSNP

Number of alleles fetched