Allele Registry

Canonical Allele Identifier: PA916037772

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000088725

RCV001543633

ClinVar Variation:

102494

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Ser350Thr	CA229304 NM_001354304.2:c.1048T>A