Canonical Allele Identifier: PA116795
Gene: NLRP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 4376

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004886.3:p.Phe575Ser
CA116792
NM_004895.5:c.1724T>C