Canonical Allele Identifier: PA2580134597
Gene: FCGR3A HGNC NCBI

Linked Data

ClinVar Variation Id: 2212560
ClinVar RCV Id: RCV004075265

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121064.2:p.Cys276Phe
CA1211385
NM_001127592.2:c.827G>T