Canonical Allele Identifier: PA2828433223
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97866
ClinVar RCV Id: RCV000320195 RCV001509517 RCV002513885 RCV001781426 RCV003964950 RCV002260986
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Ala891Asp
CA150302
NM_001370466.1:c.2672C>A