Allele Registry

Canonical Allele Identifier: PA891866504

Gene: FCGR3B HGNC NCBI

ClinVar RCV:

RCV000946516

ClinVar Variation:

242685

HGVS (amino-acid)	Matching Registered Transcripts
NP_001231682.2:p.Asn65Ser	CA044074 NM_001244753.2:c.194A>G