Allele Registry

Canonical Allele Identifier: PA106682

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089011

ClinVar Variation:

102761

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Tyr206Asp	CA229659 NM_000277.3:c.616T>G