Canonical Allele Identifier: PA2826573500
Gene: NLRP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 330018
ClinVar RCV Id: RCV000379617 RCV002263058 RCV002521246
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264058.1:p.Asp833Glu
CA9639054
NM_001277129.1:c.2499C>A
CA407409481
NM_001277129.1:c.2499C>G