Canonical Allele Identifier: PA2826573001
Gene: NLRP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 330037
ClinVar RCV Id: RCV000481155 RCV002263584 RCV001080546 RCV003922406
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264058.1:p.Thr260Met
CA9639613
NM_001277129.1:c.779C>T