Canonical Allele Identifier: PA2827924470
Gene: TF HGNC NCBI

Linked Data

ClinVar Variation Id: 12616
ClinVar RCV Id: RCV000013450 RCV001144085 RCV002513011 RCV003155024 RCV003914834
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341632.2:p.Gly627Glu
CA122561
NM_001354703.2:c.1880G>A