Allele Registry

Canonical Allele Identifier: PA916037786

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000088754

RCV000672118

ClinVar Variation:

102521

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Pro366His	CA229341 NM_001354304.2:c.1097C>A