Allele Registry

Canonical Allele Identifier: PA916037621

Gene: PAH HGNC NCBI

ClinVar Allele:

108570

ClinVar RCV:

RCV000089093

RCV000758099

ClinVar Variation:

102834

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.His264Leu	CA229761 NM_001354304.2:c.791A>T