Canonical Allele Identifier: PA2826234907
Gene: NLRC4 HGNC NCBI
ClinVar RCV:
RCV000805103
ClinVar Variation:
650029
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001186068.1:p.Val892Met
CA1601726
NM_001199139.1:c.2674G>A