Canonical Allele Identifier: PA2826572856
Gene: NLRP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 330044
ClinVar RCV Id: RCV000884290 RCV002263589 RCV002521247 RCV003957696
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264058.1:p.Pro100Ser
CA9639769
NM_001277129.1:c.298C>T