Allele Registry

Canonical Allele Identifier: PA2825138011

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV001986456

ClinVar Variation:

1491340

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Glu205Gly	CA386296709 NM_000277.3:c.614A>G