Allele Registry

Canonical Allele Identifier: PA105907

Gene: PAH HGNC NCBI

ClinVar Allele:

108612

ClinVar RCV:

RCV000089137

RCV000169005

ClinVar Variation:

102876

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Ile283Phe	CA229820 NM_000277.3:c.847A>T