Allele Registry

Canonical Allele Identifier: PA645467608

Gene: FCGR3A HGNC NCBI

ClinVar RCV:

RCV000454434

RCV001613271

ClinVar Variation:

402857

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121065.1:p.Leu66Arg	CA1211499 NM_001127593.1:c.197T>G