Allele Registry

Canonical Allele Identifier: PA124362

Gene: FCGR2A HGNC NCBI

ClinVar RCV:

RCV000015946

RCV000015947

RCV000054529

RCV000454909

ClinVar Variation:

14823

HGVS (amino-acid)	Matching Registered Transcripts
NP_067674.2:p.His166Arg	CA124361 NM_021642.5:c.497A>G