Allele Registry

Canonical Allele Identifier: PA2826572279

Gene: NLRP12 HGNC NCBI

ClinVar RCV:

RCV000249573

RCV000525814

RCV001706385

RCV002262907

ClinVar Variation:

262532

HGVS (amino-acid)	Matching Registered Transcripts
NP_001264055.1:p.His304Tyr	CA9639573 NM_001277126.2:c.910C>T