Canonical Allele Identifier: PA645479831
Gene: NLRP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 329998
ClinVar RCV Id: RCV000370362

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264055.1:p.Arg1052Pro
CA9638746
NM_001277126.2:c.3155G>C