Canonical Allele Identifier: PA2826835828
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319467
ClinVar RCV Id: RCV000377831 RCV001782829 RCV002521044
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Arg803Gln
CA8051803
NM_001293557.2:c.2408G>A