Canonical Allele Identifier: PA915954526
Gene: TF HGNC NCBI

Linked Data

ClinVar Variation Id: 343424
ClinVar RCV Id: RCV000306588 RCV000891242 RCV003972449
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001054.2:p.Ser40Asn
CA2624867
NM_001063.4:c.119G>A