Canonical Allele Identifier: PA2826835797
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319464
ClinVar RCV Id: RCV000404638 RCV001357181 RCV001782826 RCV002521041 RCV003387832
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Leu762Phe
CA8051759
NM_001293557.2:c.2284C>T