Allele Registry

Canonical Allele Identifier: PA109704

Gene: TH HGNC NCBI

ClinVar RCV:

RCV000013118

RCV002274896

ClinVar Variation:

12325

HGVS (amino-acid)	Matching Registered Transcripts
NP_954986.2:p.Leu236Pro	CA341191 NM_199292.3:c.707T>C