Allele Registry

Canonical Allele Identifier: PA916037662

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089127

RCV000632877

ClinVar Variation:

102866

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Glu280Gly	CA229808 NM_001354304.2:c.839A>G