Canonical Allele Identifier: PA2499263577
Gene: TG HGNC NCBI

Linked Data

ClinVar Variation Id: 981843
ClinVar RCV Id: RCV001374524 RCV002486006 RCV003438738
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003226.4:p.Trp1050Leu
CA4883644
NM_003235.5:c.3149G>T