Allele Registry

Canonical Allele Identifier: PA2825138182

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV003494677

ClinVar Variation:

2735932

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Pro362Leu	CA16020937 NM_000277.3:c.1085C>T