Canonical Allele Identifier: PA2826573040
Gene: NLRP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 262532
ClinVar RCV Id: RCV000249573 RCV000525814 RCV001706385 RCV002262907
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264058.1:p.His304Tyr
CA9639573
NM_001277129.1:c.910C>T