Canonical Allele Identifier: PA2580289566
Gene: TG HGNC NCBI

Linked Data

ClinVar Variation Id: 2317372
ClinVar RCV Id: RCV002919751
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003226.4:p.Ala2257Asp
CA372233907
NM_003235.5:c.6770C>A