Allele Registry

Canonical Allele Identifier: PA2827924645

Gene: TF HGNC NCBI

ClinVar RCV:

RCV000013453

ClinVar Variation:

12618

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341633.2:p.Lys519Glu	CA122565 NM_001354704.2:c.1555A>G