Allele Registry

Canonical Allele Identifier: PA1139742119

Gene: PAH HGNC NCBI

ClinVar RCV:

RCV001199976

ClinVar Variation:

932252

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341233.1:p.Arg252Pro	CA16020854 NM_001354304.2:c.755G>C