Allele Registry

Canonical Allele Identifier: PA915954554

Gene: TF HGNC NCBI

ClinVar RCV:

RCV000013458

RCV003387720

ClinVar Variation:

12623

HGVS (amino-acid)	Matching Registered Transcripts
NP_001054.2:p.Glu394Lys	CA122573 NM_001063.4:c.1180G>A