Allele Registry

Canonical Allele Identifier: PA109586

Gene: TH HGNC NCBI

ClinVar RCV:

RCV000013127

ClinVar Variation:

12334

HGVS (amino-acid)	Matching Registered Transcripts
NP_954986.2:p.Cys359Phe	CA278134 NM_199292.3:c.1076G>T