Allele Registry

Canonical Allele Identifier: PA2825137992

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV003038667

ClinVar Variation:

2113230

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Thr186Ala	CA386296870 NM_000277.3:c.556A>G