Canonical Allele Identifier: PA2826961212
Gene: NLRP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 3200707
ClinVar RCV Id: RCV004495590
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303929.1:p.Asp460Glu
CA407598743
NM_001317000.1:c.1380C>A
CA407598744
NM_001317000.1:c.1380C>G