Allele Registry

Canonical Allele Identifier: PA913195077

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000758130

ClinVar Variation:

619165

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Tyr268Cys	CA16020863 NM_000277.3:c.803A>G