Allele Registry

Canonical Allele Identifier: PA3057571485

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV004586352

ClinVar Variation:

3251908

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Gln232Leu	CA386296557 NM_001354304.2:c.695A>T