Allele Registry

Canonical Allele Identifier: PA2825253144

Gene: FCGR2B HGNC NCBI

ClinVar RCV:

RCV000005800

RCV000005801

ClinVar Variation:

5467

HGVS (amino-acid)	Matching Registered Transcripts
NP_001002273.1:p.Ile231Thr	CA117549 NM_001002273.3:c.692T>C