Allele Registry

Canonical Allele Identifier: PA044206

Gene: FCGR3B HGNC NCBI

ClinVar RCV:

RCV000946516

ClinVar Variation:

242685

HGVS (amino-acid)	Matching Registered Transcripts
NP_000561.3:p.Asn65Ser	CA044074 NM_000570.5:c.194A>G