Allele Registry

Canonical Allele Identifier: PA915954529

Gene: TF HGNC NCBI

ClinVar RCV:

RCV000013456

ClinVar Variation:

12621

HGVS (amino-acid)	Matching Registered Transcripts
NP_001054.2:p.Asp77Asn	CA122569 NM_001063.4:c.229G>A