Canonical Allele Identifier: PA658809262
Gene: NLRP12 HGNC NCBI
ClinVar RCV:
RCV000627080
ClinVar Variation:
523653
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_653288.1:p.Asp294Glu
CA9639583
NM_144687.4:c.882C>G
CA407415600
NM_144687.4:c.882C>A