Canonical Allele Identifier: PA2829113278
Gene: FCGR3A HGNC NCBI

Linked Data

ClinVar Variation Id: 14828

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373379.1:p.Leu65His
CA124372
NM_001386450.1:c.194T>A