Allele Registry

Canonical Allele Identifier: PA2826531448

Gene: FCGR3B HGNC NCBI

ClinVar RCV:

RCV000946516

ClinVar Variation:

242685

HGVS (amino-acid)	Matching Registered Transcripts
NP_001257964.2:p.Asn64Ser	CA044074 NM_001271035.2:c.191A>G