Allele Registry

Canonical Allele Identifier: PA2580231143

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV002364449

RCV003098292

ClinVar Variation:

1754238

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Phe219Tyr	CA386296623 NM_001354304.2:c.656T>A