This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.
Canonical Allele Identifier: PA2826961199
Gene: NLRP8 HGNC NCBI
ClinVar RCV:
RCV004170155
ClinVar Variation:
2319536
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303929.1:p.Thr323Met
CA9684361
NM_001317000.1:c.968C>T