Canonical Allele Identifier: PA2826835339
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 531607
ClinVar RCV Id: RCV001535611 RCV002529868
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Ser211Cys
CA395867405
NM_001293557.2:c.631A>T