Allele Registry

Canonical Allele Identifier: PA109597

Gene: TH HGNC NCBI

ClinVar RCV:

RCV000013117

ClinVar Variation:

12324

HGVS (amino-acid)	Matching Registered Transcripts
NP_954986.2:p.Gln412Lys	CA278129 NM_199292.3:c.1234C>A