Canonical Allele Identifier: PA2826835380
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319441
ClinVar RCV Id: RCV000347725 RCV001782805 RCV002261058 RCV002522857
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Ala265Val
CA8051417
NM_001293557.2:c.794C>T