Canonical Allele Identifier: PA2826234498
Gene: NLRC4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3200489
ClinVar RCV Id: RCV004493389
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186068.1:p.Phe199Leu
CA346515392
NM_001199139.1:c.597C>G
CA346515394
NM_001199139.1:c.597C>A
CA346515404
NM_001199139.1:c.595T>C