Allele Registry

Canonical Allele Identifier: PA2825151806

Gene: TH HGNC NCBI

ClinVar RCV:

RCV000013127

ClinVar Variation:

12334

HGVS (amino-acid)	Matching Registered Transcripts
NP_000351.2:p.Cys328Phe	CA278134 NM_000360.3:c.983G>T