Allele Registry

Canonical Allele Identifier: PA229777

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089102

RCV000763291

ClinVar Variation:

102843

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Ile269Asn	CA229776 NM_000277.3:c.806T>A