Canonical Allele Identifier: PA915954537
Gene: TF HGNC NCBI

Linked Data

ClinVar Variation Id: 12622

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001054.2:p.Gly277Ser
CA122571
NM_001063.4:c.829G>A