Allele Registry

Canonical Allele Identifier: PA109812

Gene: TH HGNC NCBI

ClinVar RCV:

RCV000013123

ClinVar Variation:

12330

HGVS (amino-acid)	Matching Registered Transcripts
NP_954986.2:p.Thr314Met	CA278133 NM_199292.3:c.941C>T