Allele Registry

Canonical Allele Identifier: PA106369

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000000620

RCV000078534

RCV001265833

RCV003914790

ClinVar Variation:

589

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Pro281Leu	CA220589 NM_000277.3:c.842C>T