Canonical Allele Identifier: PA210708
Gene: TG HGNC NCBI

Linked Data

ClinVar Variation Id: 12702
ClinVar RCV Id: RCV000013539

Amino-acid Alleles

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