Allele Registry

Canonical Allele Identifier: PA916037793

Gene: PAH HGNC NCBI

ClinVar Allele:

108264

ClinVar RCV:

RCV000088761

RCV000306209

ClinVar Variation:

102528

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Thr372Ser	CA229350 NM_001354304.2:c.1114A>T