Canonical Allele Identifier: PA2580289546
Gene: TG HGNC NCBI

Linked Data

ClinVar Variation Id: 2300183
ClinVar RCV Id: RCV002865893

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003226.4:p.His1901Pro
CA372234009
NM_003235.5:c.5702A>C