Allele Registry

Canonical Allele Identifier: PA109656

Gene: TG HGNC NCBI

ClinVar RCV:

RCV000013531

ClinVar Variation:

12694

HGVS (amino-acid)	Matching Registered Transcripts
NP_003226.4:p.Cys1996Ser	CA210702 NM_003235.5:c.5986T>A CA372236544 NM_003235.5:c.5987G>C