Allele Registry

Canonical Allele Identifier: PA2825138073

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV003471652

ClinVar Variation:

2677435

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Thr266Ile	CA386295316 NM_000277.3:c.797C>T