Allele Registry

Canonical Allele Identifier: PA210708

Gene: TG HGNC NCBI

ClinVar RCV:

RCV000013539

ClinVar Variation:

12702

HGVS (amino-acid)	Matching Registered Transcripts
NP_003226.4:p.Cys1077Arg	CA210707 NM_003235.5:c.3229T>C