Allele Registry

Canonical Allele Identifier: PA2825199199

Gene: FCGR3A HGNC NCBI

ClinVar RCV:

RCV000455498

ClinVar Variation:

225994

HGVS (amino-acid)	Matching Registered Transcripts
NP_000560.7:p.Phe176Val	CA1211378 NM_000569.8:c.526T>G