Allele Registry

Canonical Allele Identifier: PA645479771

Gene: NLRP12 HGNC NCBI

ClinVar RCV:

RCV000402772

RCV001091264

ClinVar Variation:

330028

HGVS (amino-acid)	Matching Registered Transcripts
NP_653288.1:p.Ala682Thr	CA9639283 NM_144687.4:c.2044G>A