Allele Registry

Canonical Allele Identifier: PA916037457

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000088934

RCV000632881

ClinVar Variation:

102686

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Arg155His	CA229559 NM_001354304.2:c.464G>A