Canonical Allele Identifier: PA2825645468
Gene: FCGR3A HGNC NCBI

Linked Data

ClinVar Variation Id: 2212560
ClinVar RCV Id: RCV004075265

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121065.1:p.Cys172Phe
CA1211385
NM_001127593.1:c.515G>T