Canonical Allele Identifier: PA915954584
Gene: TF HGNC NCBI

Linked Data

ClinVar Variation Id: 12618
ClinVar RCV Id: RCV000013453

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001054.2:p.Lys646Glu
CA122565
NM_001063.4:c.1936A>G