Canonical Allele Identifier: PA2829237716
Gene: NLRP11 HGNC NCBI

Linked Data

ClinVar Variation Id: 3200538
ClinVar RCV Id: RCV004495421

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001381823.1:p.Trp523Arg
CA9681927
NM_001394894.2:c.1567T>C
CA407586106
NM_001394894.2:c.1567T>A