Canonical Allele Identifier: PA2827263446
Gene: FCGR3A HGNC NCBI

Linked Data

ClinVar Variation Id: 14828

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316051.1:p.Leu171His
CA124372
NM_001329122.1:c.512T>A