Allele Registry

Canonical Allele Identifier: PA109800

Gene: TH HGNC NCBI

ClinVar RCV:

RCV000013122

ClinVar Variation:

12329

HGVS (amino-acid)	Matching Registered Transcripts
NP_954986.2:p.Thr276Pro	CA278132 NM_199292.3:c.826A>C