Allele Registry

Canonical Allele Identifier: PA916037658

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089124

RCV000672785

ClinVar Variation:

102863

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Thr278Ile	CA229803 NM_001354304.2:c.833C>T