Allele Registry

Canonical Allele Identifier: PA916037472

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000088947

RCV002514543

ClinVar Variation:

102699

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Ile164Thr	CA229578 NM_001354304.2:c.491T>C