Allele Registry

Canonical Allele Identifier: PA106166

Gene: PAH HGNC NCBI

ClinVar Allele:

108207

ClinVar RCV:

RCV000088702

RCV001543650

ClinVar Variation:

102471

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Lys341Thr	CA229274 NM_000277.3:c.1022A>C