Canonical Allele Identifier: PA645494258
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319458
ClinVar RCV Id: RCV000397913 RCV001782820 RCV002261061 RCV002522865
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Arg684Trp
CA8051682
NM_022162.3:c.2050C>T