Canonical Allele Identifier: PA122639
Gene: TG HGNC NCBI

Linked Data

ClinVar Variation Id: 12698
ClinVar RCV Id: RCV000013535 RCV000254213 RCV000368266 RCV001675580
ClinVar Variation Id: 2888457
ClinVar RCV Id: RCV003724903
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003226.4:p.Met1028Val
CA122638
NM_003235.5:c.3082A>G
CA2739269003
NM_003235.5:c.3081_3082delinsTG