Allele Registry

Canonical Allele Identifier: PA2830435223

Gene: TH HGNC NCBI

ClinVar RCV:

RCV000013123

ClinVar Variation:

12330

HGVS (amino-acid)	Matching Registered Transcripts
NP_954987.2:p.Thr310Met	CA278133 NM_199293.3:c.929C>T