Allele Registry

Canonical Allele Identifier: PA916037651

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089117

RCV000664652

ClinVar Variation:

102856

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Met276Val	CA229794 NM_001354304.2:c.826A>G