Allele Registry

Canonical Allele Identifier: PA2825151912

Gene: TH HGNC NCBI

ClinVar RCV:

RCV000013117

ClinVar Variation:

12324

HGVS (amino-acid)	Matching Registered Transcripts
NP_000351.2:p.Gln381Lys	CA278129 NM_000360.3:c.1141C>A