Allele Registry

Canonical Allele Identifier: PA109824

Gene: TH HGNC NCBI

ClinVar RCV:

RCV000433260

RCV001782901

ClinVar Variation:

378729

HGVS (amino-acid)	Matching Registered Transcripts
NP_954986.2:p.Thr399Met	CA16605881 NM_199292.3:c.1196C>T