Allele Registry

Canonical Allele Identifier: PA2827924652

Gene: TF HGNC NCBI

ClinVar Allele:

27655

ClinVar RCV:

RCV000013450

RCV001144085

RCV002513011

RCV003155024

RCV003914834

ClinVar Variation:

12616

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341633.2:p.Gly544Glu	CA122561 NM_001354704.2:c.1631G>A