Allele Registry

Canonical Allele Identifier: PA2826961169

Gene: NLRP8 HGNC NCBI

ClinVar Variation Id: 3200726

HGVS (amino-acid)	Matching Registered Transcripts
NP_001303929.1:p.Phe29Leu	CA407595764 NM_001317000.1:c.85T>C CA407595767 NM_001317000.1:c.87C>A CA407595768 NM_001317000.1:c.87C>G