Allele Registry

Canonical Allele Identifier: PA2825151630

Gene: TH HGNC NCBI

ClinVar RCV:

RCV000013122

ClinVar Variation:

12329

HGVS (amino-acid)	Matching Registered Transcripts
NP_000351.2:p.Thr245Pro	CA278132 NM_000360.3:c.733A>C