Allele Registry

Canonical Allele Identifier: PA2830435057

Gene: TH HGNC NCBI

ClinVar RCV:

RCV000478105

ClinVar Variation:

422210

HGVS (amino-acid)	Matching Registered Transcripts
NP_954987.2:p.Ile246Thr	CA16619300 NM_199293.3:c.737T>C