Allele Registry

Canonical Allele Identifier: PA916037626

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089096

RCV001854515

ClinVar Variation:

102837

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Thr266Ala	CA229765 NM_001354304.2:c.796A>G