Allele Registry

Canonical Allele Identifier: PA916037751

Gene: PAH HGNC NCBI

ClinVar Allele:

108209

ClinVar RCV:

RCV000088704

RCV001386152

ClinVar Variation:

102473

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Ala342Thr	CA229276 NM_001354304.2:c.1024G>A