Canonical Allele Identifier: PA2826572787
Gene: NLRP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 330048
ClinVar RCV Id: RCV000907030 RCV002263591 RCV002521248 RCV003940320
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264058.1:p.Ala5Glu
CA9639861
NM_001277129.1:c.14C>A