Canonical Allele Identifier: PA2826835901
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97866
ClinVar RCV Id: RCV000320195 RCV001509517 RCV002513885 RCV001781426 RCV003964950 RCV002260986
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Ala891Asp
CA150302
NM_001293557.2:c.2672C>A