Allele Registry

Canonical Allele Identifier: PA210701

Gene: TG HGNC NCBI

ClinVar RCV:

RCV000013530

ClinVar Variation:

12693

HGVS (amino-acid)	Matching Registered Transcripts
NP_003226.4:p.Cys1245Arg	CA210700 NM_003235.5:c.3733T>C