Allele Registry

Canonical Allele Identifier: PA2825137974

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV001375887

ClinVar Variation:

1065373

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Asn167Tyr	CA16020802 NM_000277.3:c.499A>T