Canonical Allele Identifier: PA645500009
Gene: TG HGNC NCBI

Linked Data

ClinVar Variation Id: 361926
ClinVar RCV Id: RCV000316549 RCV000434871 RCV002481241 RCV002523631
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003226.4:p.Arg854Trp
CA4883430
NM_003235.5:c.2560C>T