Canonical Allele Identifier: PA117550
Gene: FCGR2B HGNC NCBI

Linked Data

ClinVar Variation Id: 5467

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003992.3:p.Ile232Thr
CA117549
NM_004001.5:c.695T>C