Allele Registry

Canonical Allele Identifier: PA916037429

Gene: PAH HGNC NCBI

ClinVar Allele:

227029

ClinVar RCV:

RCV000210807

ClinVar Variation:

225134

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.His107Arg	CA354151 NM_001354304.2:c.320A>G