Allele Registry

Canonical Allele Identifier: PA105352

Gene: PAH HGNC NCBI

ClinVar Allele:

108418

ClinVar RCV:

RCV000088930

ClinVar Variation:

102682

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Asp151His	CA229553 NM_000277.3:c.451G>C