Allele Registry

Canonical Allele Identifier: PA269922

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000119826

ClinVar Variation:

133314

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Arg261Gly	CA269921 NM_000277.3:c.781C>G