Allele Registry

Canonical Allele Identifier: PA2825151891

Gene: TH HGNC NCBI

ClinVar RCV:

RCV000433260

RCV001782901

ClinVar Variation:

378729

HGVS (amino-acid)	Matching Registered Transcripts
NP_000351.2:p.Thr368Met	CA16605881 NM_000360.3:c.1103C>T