Allele Registry

Canonical Allele Identifier: PA915954584

Gene: TF HGNC NCBI

ClinVar RCV:

RCV000013453

ClinVar Variation:

12618

HGVS (amino-acid)	Matching Registered Transcripts
NP_001054.2:p.Lys646Glu	CA122565 NM_001063.4:c.1936A>G