Allele Registry

Canonical Allele Identifier: PA105795

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089002

RCV000806196

ClinVar Variation:

102753

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.His201Arg	CA229644 NM_000277.3:c.602A>G