Allele Registry

Canonical Allele Identifier: PA106420

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000000667

RCV000088804

ClinVar Variation:

635

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Pro407Leu	CA229402 NM_000277.3:c.1220C>T