Canonical Allele Identifier: PA2825199196
Gene: FCGR3A HGNC NCBI

Linked Data

ClinVar Variation Id: 2212560
ClinVar RCV Id: RCV004075265

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000560.7:p.Cys172Phe
CA1211385
NM_000569.8:c.515G>T