Canonical Allele Identifier: PA2827924589
Gene: TF HGNC NCBI

Linked Data

ClinVar Variation Id: 2252979
ClinVar RCV Id: RCV004107730
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341633.2:p.Leu359Val
CA2625306
NM_001354704.2:c.1075C>G