Canonical Allele Identifier: PA645500099
Gene: TG HGNC NCBI

Linked Data

ClinVar Variation Id: 423783
ClinVar RCV Id: RCV000485209
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003226.4:p.Leu1286Met
CA16618602
NM_003235.5:c.3856C>A