Allele Registry

Canonical Allele Identifier: PA916037447

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000088916

ClinVar Variation:

102668

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.His146Tyr	CA229540 NM_001354304.2:c.436C>T