Canonical Allele Identifier: PA2829979911
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 961982
ClinVar RCV Id: RCV002261314 RCV002563837
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Arg1009Gly
CA8052049
NM_022162.3:c.3025A>G