Allele Registry

Canonical Allele Identifier: PA915954555

Gene: TF HGNC NCBI

ClinVar RCV:

RCV000013455

ClinVar Variation:

12620

HGVS (amino-acid)	Matching Registered Transcripts
NP_001054.2:p.Ala477Pro	CA122567 NM_001063.4:c.1429G>C