Canonical Allele Identifier: PA2826233936
Gene: NLRC4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1000201
ClinVar RCV Id: RCV001296298
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186067.1:p.Phe253Leu
CA346514455
NM_001199138.2:c.759C>G
CA346514456
NM_001199138.2:c.759C>A
CA346514461
NM_001199138.2:c.757T>C