Allele Registry

Canonical Allele Identifier: PA2825138047

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV001897774

ClinVar Variation:

1384686

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Gln235Lys	CA386296544 NM_000277.3:c.703C>A