Canonical Allele Identifier: PA2826835713
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4693
ClinVar RCV Id: RCV000203217 RCV000365422 RCV000416493 RCV001810832 RCV001535441 RCV001781186 RCV002262557 RCV002512783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Arg675Trp
CA213414
NM_001293557.2:c.2023C>T