Allele Registry

Canonical Allele Identifier: PA916037452

Gene: PAH HGNC NCBI

ClinVar Allele:

108419

ClinVar RCV:

RCV000088931

ClinVar Variation:

102683

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Asp151Gly	CA229554 NM_001354304.2:c.452A>G