Allele Registry

Canonical Allele Identifier: PA916037365

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000758110

ClinVar Variation:

619156

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Gly46Arg	CA16020731 NM_001354304.2:c.136G>C