Allele Registry

Canonical Allele Identifier: PA2825151724

Gene: TH HGNC NCBI

ClinVar RCV:

RCV000623066

ClinVar Variation:

520940

HGVS (amino-acid)	Matching Registered Transcripts
NP_000351.2:p.Thr283Arg	CA379126409 NM_000360.3:c.848C>G