Allele Registry

Canonical Allele Identifier: PA916037832

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000088808

RCV001269318

ClinVar Variation:

102572

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Phe410Cys	CA229406 NM_001354304.2:c.1229T>G