Canonical Allele Identifier: PA2826845949
Gene: NLRP11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2298925
ClinVar RCV Id: RCV004149787
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284672.1:p.Arg383Lys
CA407586623
NM_001297743.1:c.1148G>A