Allele Registry

Canonical Allele Identifier: PA913195053

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000758131

ClinVar Variation:

619166

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Thr238Ala	CA16020847 NM_000277.3:c.712A>G