Allele Registry

Canonical Allele Identifier: PA916037576

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089053

RCV002259590

ClinVar Variation:

102802

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Phe240Ser	CA229715 NM_001354304.2:c.719T>C