Allele Registry

Canonical Allele Identifier: PA916037632

Gene: PAH HGNC NCBI

ClinVar Allele:

610550

ClinVar RCV:

RCV000758130

ClinVar Variation:

619165

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Tyr268Cys	CA16020863 NM_001354304.2:c.803A>G