Allele Registry

Canonical Allele Identifier: PA109667

Gene: TG HGNC NCBI

ClinVar RCV:

RCV000013540

ClinVar Variation:

12703

HGVS (amino-acid)	Matching Registered Transcripts
NP_003226.4:p.Gly2375Arg	CA210709 NM_003235.5:c.7123G>A CA372238177 NM_003235.5:c.7123G>C