Canonical Allele Identifier: PA2826835553
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97830
ClinVar RCV Id: RCV000084087
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Gly454Asp
CA150205
NM_001293557.2:c.1361G>A