Canonical Allele Identifier: PA122635
Gene: TG HGNC NCBI

Linked Data

ClinVar Variation Id: 12696
ClinVar RCV Id: RCV000013533 RCV000251808 RCV001723563 RCV000277644
ClinVar Variation Id: 2840391
ClinVar RCV Id: RCV003716328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003226.4:p.Arg1999Trp
CA122634
NM_003235.5:c.5995C>T
CA2739268970
NM_003235.5:c.5994_5995delinsGT