Allele Registry

Canonical Allele Identifier: PA916037722

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000994964

ClinVar Variation:

806927

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Glu319Gly	CA386291573 NM_001354304.2:c.956A>G