Allele Registry

Canonical Allele Identifier: PA2827924629

Gene: TF HGNC NCBI

ClinVar RCV:

RCV000202418

ClinVar Variation:

218294

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341633.2:p.Arg482Trp	CA211198 NM_001354704.2:c.1444C>T