Allele Registry

Canonical Allele Identifier: PA2825138175

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV001789823

ClinVar Variation:

1327561

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Ser359Leu	CA16020934 NM_000277.3:c.1076C>T