Allele Registry

Canonical Allele Identifier: PA2829228780

Gene: FCGR2B HGNC NCBI

ClinVar RCV:

RCV000005800

RCV000005801

ClinVar Variation:

5467

HGVS (amino-acid)	Matching Registered Transcripts
NP_001381406.1:p.Ile232Thr	CA117549 NM_001394477.1:c.695T>C