Canonical Allele Identifier: PA1139703914
Gene: TG HGNC NCBI

Linked Data

ClinVar Variation Id: 911985
ClinVar RCV Id: RCV001164847
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003226.4:p.Ser163Asn
CA4882934
NM_003235.5:c.488G>A