Allele Registry

Canonical Allele Identifier: PA916037762

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000088714

RCV000490440

ClinVar Variation:

102483

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Ala345Thr	CA229291 NM_001354304.2:c.1033G>A