Canonical Allele Identifier: PA2580289590
Gene: TG HGNC NCBI

Linked Data

ClinVar Variation Id: 1723792
ClinVar RCV Id: RCV002306353
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003226.4:p.Ala2713Thr
CA4885902
NM_003235.5:c.8137G>A