Allele Registry

Canonical Allele Identifier: PA2825151552

Gene: TH HGNC NCBI

ClinVar RCV:

RCV000478105

ClinVar Variation:

422210

HGVS (amino-acid)	Matching Registered Transcripts
NP_000351.2:p.Ile219Thr	CA16619300 NM_000360.3:c.656T>C