Allele Registry

Canonical Allele Identifier: PA916037667

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089136

RCV002514547

ClinVar Variation:

102875

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Asp282Gly	CA229818 NM_001354304.2:c.845A>G