Allele Registry

Canonical Allele Identifier: PA2830435544

Gene: TH HGNC NCBI

ClinVar RCV:

RCV000013119

RCV000622283

ClinVar Variation:

12326

HGVS (amino-acid)	Matching Registered Transcripts
NP_954987.2:p.Thr490Met	CA278130 NM_199293.3:c.1469C>T