Canonical Allele Identifier: PA2826572943
Gene: NLRP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 450821
ClinVar RCV Id: RCV000522253 RCV001135677 RCV002263727
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264058.1:p.Arg206Cys
CA9639659
NM_001277129.1:c.616C>T