Allele Registry

Canonical Allele Identifier: PA916037638

Gene: PAH HGNC NCBI

ClinVar Allele:

108581

ClinVar RCV:

RCV000089104

ClinVar Variation:

102845

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Arg270Gly	CA229779 NM_001354304.2:c.808A>G