Allele Registry

Canonical Allele Identifier: PA2573173226

Gene: TF HGNC NCBI

ClinVar RCV:

RCV002132157

ClinVar Variation:

1600156

HGVS (amino-acid)	Matching Registered Transcripts
NP_001054.2:p.Ile448Val	CA2625286 NM_001063.4:c.1342A>G