Canonical Allele Identifier: PA2825645510
Gene: FCGR3A HGNC NCBI

Linked Data

ClinVar Variation Id: 14828

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121068.1:p.Leu65His
CA124372
NM_001127596.2:c.194T>A