Canonical Allele Identifier: PA1139704523
Gene: TG HGNC NCBI

Linked Data

ClinVar Variation Id: 908418
ClinVar RCV Id: RCV001158914
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003226.4:p.Ser2723Leu
CA4885912
NM_003235.5:c.8168C>T