Canonical Allele Identifier: PA2829113276
Gene: FCGR3A HGNC NCBI

Linked Data

ClinVar Variation Id: 156330
ClinVar RCV Id: RCV000455042

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373379.1:p.Ser64Asn
CA233189
NM_001386450.1:c.191G>A