Canonical Allele Identifier: PA1139704123
Gene: TG HGNC NCBI

Linked Data

ClinVar Variation Id: 908085
ClinVar RCV Id: RCV001158366 RCV002483903
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003226.4:p.Asp1014His
CA4883600
NM_003235.5:c.3040G>C