Canonical Allele Identifier: PA2826845952
Gene: NLRP11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2612809
ClinVar RCV Id: RCV004356215
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284672.1:p.Ser426Leu
CA9681926
NM_001297743.1:c.1277C>T