Allele Registry

Canonical Allele Identifier: PA916037688

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000993640

ClinVar Variation:

805823

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Arg297Leu	CA16020886 NM_001354304.2:c.890G>T