Allele Registry

Canonical Allele Identifier: PA916037624

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000106367

ClinVar Variation:

120286

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Thr266Pro	CA267673 NM_001354304.2:c.796A>C