Allele Registry

Canonical Allele Identifier: PA2827924560

Gene: TF HGNC NCBI

ClinVar RCV:

RCV000013458

RCV003387720

ClinVar Variation:

12623

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341633.2:p.Glu267Lys	CA122573 NM_001354704.2:c.799G>A