Allele Registry

Canonical Allele Identifier: PA2827924401

Gene: TF HGNC NCBI

ClinVar RCV:

RCV000013455

ClinVar Variation:

12620

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341632.2:p.Ala433Pro	CA122567 NM_001354703.2:c.1297G>C