Canonical Allele Identifier: PA2741976043
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2949556
ClinVar RCV Id: RCV003804722
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Lys220Arg
CA395867292
NM_022162.3:c.659A>G