Canonical Allele Identifier: PA916027666
Gene: FCGR3A HGNC NCBI

Linked Data

ClinVar Variation Id: 14828

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316049.1:p.Leu66His
CA124372
NM_001329120.2:c.197T>A