Canonical Allele Identifier: PA210706
Gene: TG HGNC NCBI

Linked Data

ClinVar Variation Id: 12700
ClinVar RCV Id: RCV000013537 RCV001329060 RCV001551747
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003226.4:p.Arg2242His
CA210705
NM_003235.5:c.6725G>A