Allele Registry

Canonical Allele Identifier: PA2829060866

Gene: FCGR2B HGNC NCBI

ClinVar RCV:

RCV000005800

RCV000005801

ClinVar Variation:

5467

HGVS (amino-acid)	Matching Registered Transcripts
NP_001372935.1:p.Ile225Thr	CA117549 NM_001386006.1:c.674T>C