Canonical Allele Identifier: PA2741976153
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2929517
ClinVar RCV Id: RCV003784683
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Ser493Phe
CA395869008
NM_022162.3:c.1478C>T