Allele Registry

Canonical Allele Identifier: PA2830435123

Gene: TH HGNC NCBI

ClinVar RCV:

RCV000013122

ClinVar Variation:

12329

HGVS (amino-acid)	Matching Registered Transcripts
NP_954987.2:p.Thr272Pro	CA278132 NM_199293.3:c.814A>C