Allele Registry

Canonical Allele Identifier: PA229352

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000088762

RCV002259583

ClinVar Variation:

102529

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Ala373Thr	CA229351 NM_000277.3:c.1117G>A