Canonical Allele Identifier: PA2826234241
Gene: NLRC4 HGNC NCBI

Linked Data

ClinVar Variation Id: 475252
ClinVar RCV Id: RCV000546624 RCV001706673 RCV002263805 RCV002268166 RCV003925704
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186067.1:p.Gly786Val
CA1601808
NM_001199138.2:c.2357G>T