Canonical Allele Identifier: PA916008067
Gene: NLRP12 HGNC NCBI
ClinVar RCV:
RCV000370362
ClinVar Variation:
329998
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264058.1:p.Arg994Pro
CA9638746
NM_001277129.1:c.2981G>C