Allele Registry

Canonical Allele Identifier: PA658676558

Gene: NLRP12 HGNC NCBI

ClinVar Variation Id: 450821

HGVS (amino-acid)	Matching Registered Transcripts
NP_653288.1:p.Arg206Cys	CA9639659 NM_144687.4:c.616C>T