Canonical Allele Identifier: PA2826572302
Gene: NLRP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 330033
ClinVar RCV Id: RCV000264278 RCV001200246 RCV002263064 RCV004021757
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264055.1:p.Arg329Gln
CA9639550
NM_001277126.2:c.986G>A