Canonical Allele Identifier: PA2829425313
Gene: TG HGNC NCBI

Linked Data

ClinVar Variation Id: 3176627
ClinVar RCV Id: RCV004474487
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003226.4:p.Arg2707Gln
CA4885898
NM_003235.5:c.8120G>A