Allele Registry

Canonical Allele Identifier: PA2825137870

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV001990771

ClinVar Variation:

1478759

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Arg53Ser	CA6749039 NM_000277.3:c.157C>A