Allele Registry

Canonical Allele Identifier: PA916037702

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000000649

RCV000089157

RCV000169485

ClinVar Variation:

618

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Ile306Val	CA114365 NM_001354304.2:c.916A>G