Allele Registry

Canonical Allele Identifier: PA2830435219

Gene: TH HGNC NCBI

ClinVar RCV:

RCV000623066

ClinVar Variation:

520940

HGVS (amino-acid)	Matching Registered Transcripts
NP_954987.2:p.Thr310Arg	CA379126409 NM_199293.3:c.929C>G