Canonical Allele Identifier: PA645494252
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319456
ClinVar RCV Id: RCV000339948 RCV001782818 RCV001812848 RCV002261060 RCV002522864
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Pro668Leu
CA8051668
NM_022162.3:c.2003C>T