Canonical Allele Identifier: PA645479831
Gene: NLRP12 HGNC NCBI
ClinVar RCV:
RCV000370362
ClinVar Variation:
329998
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264055.1:p.Arg1052Pro
CA9638746
NM_001277126.2:c.3155G>C