Allele Registry

Canonical Allele Identifier: PA2825151509

Gene: TH HGNC NCBI

ClinVar RCV:

RCV000013118

RCV002274896

ClinVar Variation:

12325

HGVS (amino-acid)	Matching Registered Transcripts
NP_000351.2:p.Leu205Pro	CA341191 NM_000360.3:c.614T>C