Allele Registry

Canonical Allele Identifier: PA105842

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000088947

RCV002514543

ClinVar Variation:

102699

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Ile164Thr	CA229578 NM_000277.3:c.491T>C