Allele Registry

Canonical Allele Identifier: PA916037644

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV000758093

ClinVar Variation:

619148

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Ser273Pro	CA16020866 NM_001354304.2:c.817T>C