Allele Registry

Canonical Allele Identifier: PA916037374

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000106347

ClinVar Variation:

120266

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Phe55Ser	CA267639 NM_001354304.2:c.164T>C