Canonical Allele Identifier: PA2826573167
Gene: NLRP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 330031
ClinVar RCV Id: RCV000645634
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264058.1:p.Pro450Leu
CA9639446
NM_001277129.1:c.1349C>T