Allele Registry

Canonical Allele Identifier: PA2825152094

Gene: TH HGNC NCBI

ClinVar RCV:

RCV000013119

RCV000622283

ClinVar Variation:

12326

HGVS (amino-acid)	Matching Registered Transcripts
NP_000351.2:p.Thr463Met	CA278130 NM_000360.3:c.1388C>T