Allele Registry

Canonical Allele Identifier: PA916037630

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000672289

ClinVar Variation:

556296

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Gln267Arg	CA16020862 NM_001354304.2:c.800A>G