Allele Registry

Canonical Allele Identifier: PA2825151771

Gene: TH HGNC NCBI

ClinVar RCV:

RCV000013121

ClinVar Variation:

12328

HGVS (amino-acid)	Matching Registered Transcripts
NP_000351.2:p.Arg306His	CA278131 NM_000360.3:c.917G>A