Allele Registry

Canonical Allele Identifier: PA2825137982

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV003041168

ClinVar Variation:

2137408

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Ile174Asn	CA6748896 NM_000277.3:c.521T>A