Allele Registry

Canonical Allele Identifier: PA229421

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000088820

RCV001388783

ClinVar Variation:

102582

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Ile421Thr	CA229420 NM_000277.3:c.1262T>C