Canonical Allele Identifier: PA645494291
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 267317
ClinVar RCV Id: RCV000258046
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Val816Ile
CA10590109
NM_022162.3:c.2446G>A