Allele Registry

Canonical Allele Identifier: PA916027666

Gene: FCGR3A HGNC NCBI

ClinVar RCV:

RCV000015953

RCV000454581

ClinVar Variation:

14828

HGVS (amino-acid)	Matching Registered Transcripts
NP_001316049.1:p.Leu66His	CA124372 NM_001329120.2:c.197T>A