Allele Registry

Canonical Allele Identifier: PA106552

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000088725

RCV001543633

ClinVar Variation:

102494

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Ser350Thr	CA229304 NM_000277.3:c.1048T>A