Allele Registry

Canonical Allele Identifier: PA2825137880

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV002260502

ClinVar Variation:

1693243

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Glu66Lys	CA16020744 NM_000277.3:c.196G>A