Canonical Allele Identifier: PA2827924521
Gene: TF HGNC NCBI

Linked Data

ClinVar Variation Id: 12622

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341633.2:p.Gly150Ser
CA122571
NM_001354704.2:c.448G>A