Allele Registry

Canonical Allele Identifier: PA913194994

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000758110

ClinVar Variation:

619156

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Gly46Arg	CA16020731 NM_000277.3:c.136G>C