Canonical Allele Identifier: PA2826572270
Gene: NLRP12 HGNC NCBI
ClinVar RCV:
RCV000627080
ClinVar Variation:
523653
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264055.1:p.Asp294Glu
CA9639583
NM_001277126.2:c.882C>G
CA407415600
NM_001277126.2:c.882C>A