ClinGen Allele Registry
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Canonical Allele Identifier:
PA1139743960
Gene: FCGR2A
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000015946
RCV000015947
RCV000054529
RCV000454909
ClinVar Variation:
14823
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001362225.1:p.His167Arg
CA124361
NM_001375296.1:c.500A>G