Allele Registry

Canonical Allele Identifier: PA2741867139

Gene: PAH HGNC NCBI

ClinVar Allele:

2836305

ClinVar RCV:

RCV003471652

ClinVar Variation:

2677435

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Thr266Ile	CA386295316 NM_001354304.2:c.797C>T