Allele Registry

Canonical Allele Identifier: PA2829060767

Gene: FCGR2B HGNC NCBI

ClinVar RCV:

RCV000005800

RCV000005801

ClinVar Variation:

5467

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372929.1:p.Ile224Thr	CA117549 NM_001386000.1:c.671T>C