Canonical Allele Identifier: PA2826573033
Gene: NLRP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 523653
ClinVar RCV Id: RCV000627080
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264058.1:p.Asp294Glu
CA9639583
NM_001277129.1:c.882C>G
CA407415600
NM_001277129.1:c.882C>A