Allele Registry

Canonical Allele Identifier: PA229764

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089095

RCV000810805

ClinVar Variation:

102836

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Cys265Tyr	CA229763 NM_000277.3:c.794G>A