Allele Registry

Canonical Allele Identifier: PA916037414

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000088886

RCV001857430

ClinVar Variation:

102641

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Pro89Ser	CA229501 NM_001354304.2:c.265C>T