Canonical Allele Identifier: PA916039212
Gene: TF HGNC NCBI

Linked Data

ClinVar Variation Id: 343430

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341632.2:p.Thr68Ala
CA2624956
NM_001354703.2:c.202A>G