Allele Registry

Canonical Allele Identifier: PA916037552

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000089028

RCV001261644

ClinVar Variation:

102777

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Ile224Thr	CA229682 NM_001354304.2:c.671T>C