Allele Registry

Canonical Allele Identifier: PA2827924522

Gene: TF HGNC NCBI

ClinVar RCV:

RCV000013448

ClinVar Variation:

12614

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341633.2:p.Gly150Asp	CA122557 NM_001354704.2:c.449G>A