Allele Registry

Canonical Allele Identifier: PA916037373

Gene: PAH HGNC NCBI

ClinVar Allele:

108339

ClinVar RCV:

RCV000088844

RCV002509217

ClinVar Variation:

102603

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Phe55del	CA229450 NM_001354304.2:c.163_165del