Canonical Allele Identifier: PA2826573023
Gene: NLRP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 1522275
ClinVar RCV Id: RCV002046519

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264058.1:p.Val285Ala
CA310070968
NM_001277129.1:c.854T>C