Allele Registry

Canonical Allele Identifier: PA2825138106

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000993640

ClinVar Variation:

805823

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Arg297Leu	CA16020886 NM_000277.3:c.890G>T