Canonical Allele Identifier: PA2573278361
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1429314
ClinVar RCV Id: RCV002560633

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.His496Arg
CA395869027
NM_022162.3:c.1487A>G