Allele Registry

Canonical Allele Identifier: PA916037656

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089122

RCV001789762

ClinVar Variation:

102861

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Thr278Ala	CA229801 NM_001354304.2:c.832A>G