Canonical Allele Identifier: PA2826572950
Gene: NLRP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 330040
ClinVar RCV Id: RCV001002447 RCV003910271 RCV002263586
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264058.1:p.Pro210Leu
CA9639652
NM_001277129.1:c.629C>T