Canonical Allele Identifier: PA2826845951
Gene: NLRP11 HGNC NCBI

Linked Data

ClinVar Variation Id: 3200538
ClinVar RCV Id: RCV004495421
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284672.1:p.Trp424Arg
CA9681927
NM_001297743.1:c.1270T>C
CA407586106
NM_001297743.1:c.1270T>A