Allele Registry

Canonical Allele Identifier: PA1139742171

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV001199998

ClinVar Variation:

932267

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Phe299Ser	CA16020887 NM_001354304.2:c.896T>C