Canonical Allele Identifier: PA658674792
Gene: TG HGNC NCBI

Linked Data

ClinVar Variation Id: 450216
ClinVar RCV Id: RCV000523933

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003226.4:p.Cys160Ser
CA4882932
NM_003235.5:c.479G>C
CA372247061
NM_003235.5:c.478T>A