Canonical Allele Identifier: PA2499263586
Gene: TG HGNC NCBI

Linked Data

ClinVar Variation Id: 1214076
ClinVar RCV Id: RCV001580837 RCV002573310
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003226.4:p.Ser2716Phe
CA4885905
NM_003235.5:c.8147C>T