Allele Registry

Canonical Allele Identifier: PA2827924282

Gene: TF HGNC NCBI

ClinVar RCV:

RCV000013456

ClinVar Variation:

12621

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341632.2:p.Asp33Asn	CA122569 NM_001354703.2:c.97G>A