Allele Registry

Canonical Allele Identifier: PA2825138136

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000994964

ClinVar Variation:

806927

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Glu319Gly	CA386291573 NM_000277.3:c.956A>G