Allele Registry

Canonical Allele Identifier: PA106496

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089151

RCV000993625

ClinVar Variation:

102889

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Ser303Pro	CA229841 NM_000277.3:c.907T>C