Canonical Allele Identifier: PA102985
Gene: FCGR3A HGNC NCBI

Linked Data

ClinVar Variation Id: 14828

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121065.1:p.Leu66His
CA124372
NM_001127593.1:c.197T>A