Allele Registry

Canonical Allele Identifier: PA2827924575

Gene: TF HGNC NCBI

ClinVar RCV:

RCV002132157

ClinVar Variation:

1600156

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341633.2:p.Ile321Val	CA2625286 NM_001354704.2:c.961A>G