Canonical Allele Identifier: PA2826234959
Gene: NLRC4 HGNC NCBI

Linked Data

ClinVar Variation Id: 656380
ClinVar RCV Id: RCV000812783 RCV001172136 RCV002538133
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186068.1:p.Lys975Asn
CA1601645
NM_001199139.1:c.2925A>C
CA346519310
NM_001199139.1:c.2925A>T