Canonical Allele Identifier: PA2826573423
Gene: NLRP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 536936
ClinVar RCV Id: RCV000645651 RCV002263889
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264058.1:p.Gly736Arg
CA9639189
NM_001277129.1:c.2206G>A
CA407411209
NM_001277129.1:c.2206G>C