Allele Registry

Canonical Allele Identifier: PA2830435289

Gene: TH HGNC NCBI

ClinVar RCV:

RCV000013121

ClinVar Variation:

12328

HGVS (amino-acid)	Matching Registered Transcripts
NP_954987.2:p.Arg333His	CA278131 NM_199293.3:c.998G>A