Canonical Allele Identifier: PA174440
Gene: TG HGNC NCBI

Linked Data

ClinVar Variation Id: 161608
ClinVar RCV Id: RCV000149144
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003226.4:p.Phe1296Ile
CA174439
NM_003235.5:c.3886T>A