Allele Registry

Canonical Allele Identifier: PA2825138087

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV001199979

ClinVar Variation:

932254

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Thr278Ser	CA16020867 NM_000277.3:c.833C>G CA386294538 NM_000277.3:c.832A>T