Allele Registry

Canonical Allele Identifier: PA2573071349

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV001789827

ClinVar Variation:

1327565

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Lys361Gln	CA16020936 NM_001354304.2:c.1081A>C