Allele Registry

Canonical Allele Identifier: PA229774

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089100

RCV000758117

ClinVar Variation:

102841

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Tyr268His	CA229773 NM_000277.3:c.802T>C