Canonical Allele Identifier: PA2825645450
Gene: FCGR3A HGNC NCBI

Linked Data

ClinVar Variation Id: 3094073
ClinVar RCV Id: RCV004391427

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121064.2:p.Val221Ala
CA343368385
NM_001127592.2:c.662T>C