Allele Registry

Canonical Allele Identifier: PA913195051

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000758123

ClinVar Variation:

619160

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Gln232Glu	CA16020842 NM_000277.3:c.694C>G