Allele Registry

Canonical Allele Identifier: PA916037737

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089194

ClinVar Variation:

102927

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Gly332Glu	CA229897 NM_001354304.2:c.995G>A