Allele Registry

Canonical Allele Identifier: PA2826572317

Gene: NLRP12 HGNC NCBI

ClinVar RCV:

RCV000509371

RCV000819856

ClinVar Variation:

440985

HGVS (amino-acid)	Matching Registered Transcripts
NP_001264055.1:p.Arg343Trp	CA9639538 NM_001277126.2:c.1027C>T