Canonical Allele Identifier: PA2826835442
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97902
ClinVar RCV Id: RCV000084160 RCV002262685 RCV001753488 RCV002513891
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Arg346Cys
CA150374
NM_001293557.2:c.1036C>T