Allele Registry

Canonical Allele Identifier: PA2830435552

Gene: TH HGNC NCBI

ClinVar RCV:

RCV000364341

ClinVar Variation:

304067

HGVS (amino-acid)	Matching Registered Transcripts
NP_954987.2:p.Asp494Gly	CA5818249 NM_199293.3:c.1481A>G