Canonical Allele Identifier: PA2829237717
Gene: NLRP11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2612809
ClinVar RCV Id: RCV004356215
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001381823.1:p.Ser525Leu
CA9681926
NM_001394894.2:c.1574C>T