Allele Registry

Canonical Allele Identifier: PA915954552

Gene: TF HGNC NCBI

ClinVar RCV:

RCV000013449

RCV000390823

RCV000908694

ClinVar Variation:

12615

HGVS (amino-acid)	Matching Registered Transcripts
NP_001054.2:p.His319Arg	CA122559 NM_001063.4:c.956A>G