Allele Registry

Canonical Allele Identifier: PA2825138083

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV001252100

RCV003382491

ClinVar Variation:

975467

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Lys274Arg	CA386294555 NM_000277.3:c.821A>G