Allele Registry

Canonical Allele Identifier: PA916037661

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089125

RCV001857433

ClinVar Variation:

102864

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Glu280Gln	CA229805 NM_001354304.2:c.838G>C