Allele Registry

Canonical Allele Identifier: PA267672

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000106366

ClinVar Variation:

120285

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Val262Gly	CA267671 NM_000277.3:c.785T>G