Allele Registry

Canonical Allele Identifier: PA2825138025

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV001200013

ClinVar Variation:

932276

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.His220Pro	CA16020832 NM_000277.3:c.659A>C