Allele Registry

Canonical Allele Identifier: PA2741867153

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV003476589

ClinVar Variation:

2677442

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Ser310Cys	CA386291704 NM_001354304.2:c.929C>G