Allele Registry

Canonical Allele Identifier: PA106313

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089016

RCV000411219

RCV001192748

ClinVar Variation:

102766

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Pro211Thr	CA229666 NM_000277.3:c.631C>A