Allele Registry

Canonical Allele Identifier: PA341193

Gene: TH HGNC NCBI

ClinVar RCV:

RCV000013120

RCV000724645

ClinVar Variation:

12327

HGVS (amino-acid)	Matching Registered Transcripts
NP_000351.2:p.Arg202His	CA341192 NM_000360.3:c.605G>A