Allele Registry

Canonical Allele Identifier: PA106469

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089038

RCV001857431

ClinVar Variation:

102787

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Ser231Phe	CA229695 NM_000277.3:c.692C>T