Canonical Allele Identifier: PA658818305
Gene: NLRP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 536936
ClinVar RCV Id: RCV000645651 RCV002263889
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264055.1:p.Gly737Arg
CA9639189
NM_001277126.2:c.2209G>A
CA407411209
NM_001277126.2:c.2209G>C