Allele Registry

Canonical Allele Identifier: PA2827924447

Gene: TF HGNC NCBI

ClinVar RCV:

RCV000202418

ClinVar Variation:

218294

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341632.2:p.Arg565Trp	CA211198 NM_001354703.2:c.1693C>T