Allele Registry

Canonical Allele Identifier: PA117550

Gene: FCGR2B HGNC NCBI

ClinVar RCV:

RCV000005800

RCV000005801

ClinVar Variation:

5467

HGVS (amino-acid)	Matching Registered Transcripts
NP_003992.3:p.Ile232Thr	CA117549 NM_004001.5:c.695T>C