Canonical Allele Identifier: PA2825645519
Gene: FCGR3A HGNC NCBI

Linked Data

ClinVar Variation Id: 2212560
ClinVar RCV Id: RCV004075265

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121068.1:p.Cys171Phe
CA1211385
NM_001127596.2:c.512G>T