Allele Registry

Canonical Allele Identifier: PA229869

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089172

ClinVar Variation:

102908

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Asp315Tyr	CA229868 NM_000277.3:c.943G>T