Allele Registry

Canonical Allele Identifier: PA2825137993

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV002047826

ClinVar Variation:

1504560

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Thr186Ile	CA386296861 NM_000277.3:c.557C>T