Allele Registry

Canonical Allele Identifier: PA3057571472

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV004586231

ClinVar Variation:

3251787

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Arg53Gly	CA386302298 NM_001354304.2:c.157C>G