Allele Registry

Canonical Allele Identifier: PA916037806

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000106341

ClinVar Variation:

120260

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Val388Ala	CA267628 NM_001354304.2:c.1163T>C