Canonical Allele Identifier: PA2826961224
Gene: NLRP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2343958
ClinVar RCV Id: RCV004186142
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303929.1:p.Tyr551Ser
CA9684501
NM_001317000.1:c.1652A>C