Canonical Allele Identifier: PA2825199189
Gene: FCGR3A HGNC NCBI

Linked Data

ClinVar Variation Id: 3094078
ClinVar RCV Id: RCV004391432
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000560.7:p.Ala162Thr
CA1211393
NM_000569.8:c.484G>A