Canonical Allele Identifier: PA645500054
Gene: TG HGNC NCBI

Linked Data

ClinVar Variation Id: 361944
ClinVar RCV Id: RCV000272792

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003226.4:p.Arg1081Gly
CA10630302
NM_003235.5:c.3241C>G