Allele Registry

Canonical Allele Identifier: PA2825138085

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV003079148

ClinVar Variation:

2152159

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Met276Thr	CA6748837 NM_000277.3:c.827T>C