Canonical Allele Identifier: PA2825645489
Gene: FCGR3A HGNC NCBI

Linked Data

ClinVar Variation Id: 3094073
ClinVar RCV Id: RCV004391427
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121067.1:p.Val117Ala
CA343368385
NM_001127595.2:c.350T>C