Canonical Allele Identifier: PA1139704519
Gene: TG HGNC NCBI

Linked Data

ClinVar Variation Id: 908417
ClinVar RCV Id: RCV001158913 RCV003718373
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003226.4:p.Ala2692Val
CA4885888
NM_003235.5:c.8075C>T