Allele Registry

Canonical Allele Identifier: PA229648

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089004

RCV001543658

ClinVar Variation:

102755

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Cys203Trp	CA229647 NM_000277.3:c.609C>G