Canonical Allele Identifier: PA2826234928
Gene: NLRC4 HGNC NCBI

Linked Data

ClinVar Variation Id: 475254
ClinVar RCV Id: RCV000546974 RCV001821634 RCV002263807 RCV002263806 RCV003925705
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186068.1:p.Ala929Ser
CA1601670
NM_001199139.1:c.2785G>T