Allele Registry

Canonical Allele Identifier: PA102985

Gene: FCGR3A HGNC NCBI

ClinVar RCV:

RCV000015953

RCV000454581

ClinVar Variation:

14828

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121065.1:p.Leu66His	CA124372 NM_001127593.1:c.197T>A