Allele Registry

Canonical Allele Identifier: PA109535

Gene: TH HGNC NCBI

ClinVar RCV:

RCV000013121

ClinVar Variation:

12328

HGVS (amino-acid)	Matching Registered Transcripts
NP_954986.2:p.Arg337His	CA278131 NM_199292.3:c.1010G>A