Allele Registry

Canonical Allele Identifier: PA2825138081

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV003599095

ClinVar Variation:

2816125

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.His271Asn	CA386294570 NM_000277.3:c.811C>A