Canonical Allele Identifier: PA231731
Gene: NLRP9 HGNC NCBI

Linked Data

ClinVar Variation Id: 132878
ClinVar RCV Id: RCV000119315
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789790.2:p.Ser7Leu
CA231730
NM_176820.4:c.20C>T