Allele Registry

Canonical Allele Identifier: PA2830360020

Gene: NLRP8 HGNC NCBI

ClinVar Variation Id: 3200726

HGVS (amino-acid)	Matching Registered Transcripts
NP_789781.2:p.Phe29Leu	CA407595764 NM_176811.2:c.85T>C CA407595767 NM_176811.2:c.87C>A CA407595768 NM_176811.2:c.87C>G