Allele Registry

Canonical Allele Identifier: PA2825138276

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV003155771

ClinVar Variation:

2445852

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Ser439Gly	CA242743409 NM_000277.3:c.1315A>G