Allele Registry

Canonical Allele Identifier: PA229612

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000088977

ClinVar Variation:

102728

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Glu178Val	CA229611 NM_000277.3:c.533A>T