Allele Registry

Canonical Allele Identifier: PA2499251811

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV001375887

ClinVar Variation:

1065373

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Asn167Tyr	CA16020802 NM_001354304.2:c.499A>T