Canonical Allele Identifier: PA122637
Gene: TG HGNC NCBI

Linked Data

ClinVar Variation Id: 12697
ClinVar RCV Id: RCV000013534 RCV000253912 RCV000309189 RCV003660759
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003226.4:p.Ser734Ala
CA122636
NM_003235.5:c.2200T>G