Allele Registry

Canonical Allele Identifier: PA2825138228

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV001236942

ClinVar Variation:

962987

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Lys396Arg	CA6748729 NM_000277.3:c.1187A>G