Canonical Allele Identifier: PA150258
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97848
ClinVar RCV Id: RCV000084105 RCV000785151 RCV001781418 RCV002514478 RCV002260978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Glu778Lys
CA150256
NM_022162.3:c.2332G>A