Canonical Allele Identifier: PA645499945
Gene: TG HGNC NCBI

Linked Data

ClinVar Variation Id: 361909

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003226.4:p.Ala185Val
CA4882950
NM_003235.5:c.554C>T