Allele Registry

Canonical Allele Identifier: PA658655069

Gene: NLRP12 HGNC NCBI

ClinVar RCV:

RCV000509371

RCV000819856

ClinVar Variation:

440985

HGVS (amino-acid)	Matching Registered Transcripts
NP_653288.1:p.Arg343Trp	CA9639538 NM_144687.4:c.1027C>T