Canonical Allele Identifier: PA645479817
Gene: NLRP12 HGNC NCBI

Linked Data

ClinVar Variation Id: 330017
ClinVar RCV Id: RCV000823537 RCV001548731 RCV002263057 RCV002521245
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264055.1:p.Arg860Trp
CA9639038
NM_001277126.2:c.2578C>T