Allele Registry

Canonical Allele Identifier: PA2825138217

Gene: PAH HGNC NCBI

ClinVar Allele:

1318157

ClinVar RCV:

RCV001789815

ClinVar Variation:

1327553

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Tyr387Asp	CA16020952 NM_000277.3:c.1159T>G