Allele Registry

Canonical Allele Identifier: PA2825138133

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV001974670

ClinVar Variation:

1436015

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Tyr317Cys	CA386291606 NM_000277.3:c.950A>G