Allele Registry

Canonical Allele Identifier: PA106206

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000088945

RCV000674841

ClinVar Variation:

102697

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Phe161Ser	CA229575 NM_000277.3:c.482T>C