Canonical Allele Identifier: PA2825645444
Gene: FCGR3A HGNC NCBI

Linked Data

ClinVar Variation Id: 14828

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121064.2:p.Leu170His
CA124372
NM_001127592.2:c.509T>A