Allele Registry

Canonical Allele Identifier: PA109566

Gene: TH HGNC NCBI

ClinVar RCV:

RCV000364341

ClinVar Variation:

304067

HGVS (amino-acid)	Matching Registered Transcripts
NP_954986.2:p.Asp498Gly	CA5818249 NM_199292.3:c.1493A>G