Allele Registry

Canonical Allele Identifier: PA229766

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089096

RCV001854515

ClinVar Variation:

102837

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Thr266Ala	CA229765 NM_000277.3:c.796A>G