Allele Registry

Canonical Allele Identifier: PA2825138123

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV003476589

ClinVar Variation:

2677442

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Ser310Cys	CA386291704 NM_000277.3:c.929C>G