Canonical Allele Identifier: PA2829978816
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2930801
ClinVar RCV Id: RCV003790111

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.His126Asn
CA395866419
NM_022162.3:c.376C>A