Allele Registry

Canonical Allele Identifier: PA916037817

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000088783

RCV000410586

ClinVar Variation:

102549

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Ala395Gly	CA286498 NM_001354304.2:c.1184C>G