Allele Registry

Canonical Allele Identifier: PA915954572

Gene: TF HGNC NCBI

ClinVar RCV:

RCV000202418

ClinVar Variation:

218294

HGVS (amino-acid)	Matching Registered Transcripts
NP_001054.2:p.Arg609Trp	CA211198 NM_001063.4:c.1825C>T