Allele Registry

Canonical Allele Identifier: PA916037724

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089176

RCV000797233

RCV002515784

ClinVar Variation:

102912

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Ala322Thr	CA229875 NM_001354304.2:c.964G>A