Canonical Allele Identifier: PA116794
Gene: NLRP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 4376

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230062.1:p.Phe573Ser
CA116792
NM_001243133.2:c.1718T>C