Allele Registry

Canonical Allele Identifier: PA2741867155

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV003404748

ClinVar Variation:

2637450

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Leu321Ile	CA386291549 NM_001354304.2:c.961C>A