Allele Registry

Canonical Allele Identifier: PA229864

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089168

RCV000672630

ClinVar Variation:

102904

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Pro314Thr	CA229863 NM_000277.3:c.940C>A