Allele Registry

Canonical Allele Identifier: PA229796

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089118

RCV000758121

ClinVar Variation:

102857

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Met276Lys	CA229795 NM_000277.3:c.827T>A