Allele Registry

Canonical Allele Identifier: PA916037633

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089100

RCV000758117

ClinVar Variation:

102841

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Tyr268His	CA229773 NM_001354304.2:c.802T>C