Allele Registry

Canonical Allele Identifier: PA2825137991

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV003496597

ClinVar Variation:

2765012

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Lys185Glu	CA386296889 NM_000277.3:c.553A>G