Allele Registry

Canonical Allele Identifier: PA916037625

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089097

ClinVar Variation:

102838

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Thr266Lys	CA229767 NM_001354304.2:c.797C>A