Allele Registry

Canonical Allele Identifier: PA105029

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000088935

RCV000675156

ClinVar Variation:

102687

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Arg155Pro	CA229561 NM_000277.3:c.464G>C