Canonical Allele Identifier: PA2826835769
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 644507
ClinVar RCV Id: RCV002537091 RCV002537090
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Glu721Lys
CA8051735
NM_001293557.2:c.2161G>A