Allele Registry

Canonical Allele Identifier: PA106625

Gene: PAH HGNC NCBI

ClinVar Allele:

108264

ClinVar RCV:

RCV000088761

RCV000306209

ClinVar Variation:

102528

HGVS (amino-acid)	Matching Registered Transcripts
NP_000268.1:p.Thr372Ser	CA229350 NM_000277.3:c.1114A>T