Canonical Allele Identifier: PA2826835537
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4695
ClinVar RCV Id: RCV000004959
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Leu442Phe
CA117020
NM_001293557.2:c.1324C>T