Allele Registry

Canonical Allele Identifier: PA2825138019

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV002601709

ClinVar Variation:

1917938

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Cys217Phe	CA386296634 NM_000277.3:c.650G>T