Canonical Allele Identifier: PA2826835467
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 531599
ClinVar RCV Id: RCV001118317 RCV001784213 RCV002263872 RCV002528894 RCV001811129 RCV003905719
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Pro370Leu
CA8051488
NM_001293557.2:c.1109C>T