Canonical Allele Identifier: PA2826573083
Gene: NLRP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 523654
ClinVar RCV Id: RCV000627081 RCV001311905 RCV002263840
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264058.1:p.Arg352Cys
CA9639530
NM_001277129.1:c.1054C>T