Allele Registry

Canonical Allele Identifier: PA916037425

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000669128

ClinVar Variation:

553638

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Gly103Cys	CA6748984 NM_001354304.2:c.307G>T