Allele Registry

Canonical Allele Identifier: PA2825152109

Gene: TH HGNC NCBI

ClinVar RCV:

RCV000364341

ClinVar Variation:

304067

HGVS (amino-acid)	Matching Registered Transcripts
NP_000351.2:p.Asp467Gly	CA5818249 NM_000360.3:c.1400A>G