Canonical Allele Identifier: PA2830256476
Gene: NLRP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 330022
ClinVar RCV Id: RCV000893516 RCV004021756 RCV003910270
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653288.1:p.Lys770Thr
CA9639120
NM_144687.4:c.2309A>C