Allele Registry

Canonical Allele Identifier: PA2826572607

Gene: NLRP12 HGNC NCBI

ClinVar RCV:

RCV000402772

RCV001091264

ClinVar Variation:

330028

HGVS (amino-acid)	Matching Registered Transcripts
NP_001264055.1:p.Ala682Thr	CA9639283 NM_001277126.2:c.2044G>A