Allele Registry

Canonical Allele Identifier: PA109508

Gene: TH HGNC NCBI

ClinVar RCV:

RCV000013120

RCV000724645

ClinVar Variation:

12327

HGVS (amino-acid)	Matching Registered Transcripts
NP_954986.2:p.Arg233His	CA341192 NM_199292.3:c.698G>A