Canonical Allele Identifier: PA2580289589
Gene: TG HGNC NCBI

Linked Data

ClinVar Variation Id: 2267294
ClinVar RCV Id: RCV002803987
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003226.4:p.Ser2701Gly
CA186356750
NM_003235.5:c.8101A>G