Allele Registry

Canonical Allele Identifier: PA3057571478

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV005240177

ClinVar Variation:

3769446

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Tyr168Asn	CA386299477 NM_001354304.2:c.502T>A