Canonical Allele Identifier: PA2825395897
Gene: TF HGNC NCBI

Linked Data

ClinVar Variation Id: 343430

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001054.2:p.Thr112Ala
CA2624956
NM_001063.4:c.334A>G