Allele Registry

Canonical Allele Identifier: PA2573071353

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV001789809

ClinVar Variation:

1327547

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Asp415Tyr	CA16020978 NM_001354304.2:c.1243G>T