Allele Registry

Canonical Allele Identifier: PA2826531487

Gene: FCGR3B HGNC NCBI

ClinVar RCV:

RCV000946516

ClinVar Variation:

242685

HGVS (amino-acid)	Matching Registered Transcripts
NP_001257966.1:p.Asn48Ser	CA044074 NM_001271037.2:c.143A>G