Allele Registry

Canonical Allele Identifier: PA645479766

Gene: NLRP12 HGNC NCBI

ClinVar RCV:

RCV000645634

ClinVar Variation:

330031

HGVS (amino-acid)	Matching Registered Transcripts
NP_653288.1:p.Pro450Leu	CA9639446 NM_144687.4:c.1349C>T