Allele Registry

Canonical Allele Identifier: PA109618

Gene: TG HGNC NCBI

ClinVar RCV:

RCV000013542

RCV002496347

RCV003556011

ClinVar Variation:

12705

HGVS (amino-acid)	Matching Registered Transcripts
NP_003226.4:p.Arg2336Gln	CA210711 NM_003235.5:c.7007G>A