Allele Registry

Canonical Allele Identifier: PA658811295

Gene: TH HGNC NCBI

ClinVar RCV:

RCV000623066

ClinVar Variation:

520940

HGVS (amino-acid)	Matching Registered Transcripts
NP_954986.2:p.Thr314Arg	CA379126409 NM_199292.3:c.941C>G