Allele Registry

Canonical Allele Identifier: PA229843

Gene: PAH HGNC NCBI

ClinVar Allele:

108626

ClinVar RCV:

RCV000089152

RCV001543639

ClinVar Variation:

102890

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Ser303Ala	CA229842 NM_000277.3:c.907T>G