Allele Registry

Canonical Allele Identifier: PA106410

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000088754

RCV000672118

ClinVar Variation:

102521

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Pro366His	CA229341 NM_000277.3:c.1097C>A