Allele Registry

Canonical Allele Identifier: PA106605

Gene: PAH HGNC NCBI

ClinVar Allele:

108597

ClinVar RCV:

RCV000089122

RCV001789762

ClinVar Variation:

102861

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Thr278Ala	CA229801 NM_000277.3:c.832A>G