Allele Registry

Canonical Allele Identifier: PA916037736

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000410352

ClinVar Variation:

371278

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Phe331Ser	CA16020915 NM_001354304.2:c.992T>C