Allele Registry

Canonical Allele Identifier: PA2826166237

Gene: FCGR2B HGNC NCBI

ClinVar RCV:

RCV000005800

RCV000005801

ClinVar Variation:

5467

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177757.1:p.Ile225Thr	CA117549 NM_001190828.2:c.674T>C