Allele Registry

Canonical Allele Identifier: PA916037573

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089048

ClinVar Variation:

102797

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Gly239Ser	CA229706 NM_001354304.2:c.715G>A