Canonical Allele Identifier: PA2580289484
Gene: TG HGNC NCBI

Linked Data

ClinVar Variation Id: 2369374
ClinVar RCV Id: RCV003001196

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003226.4:p.Arg170Pro
CA4882938
NM_003235.5:c.509G>C