Canonical Allele Identifier: PA645494270
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319460

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Arg716His
CA8051707
NM_022162.3:c.2147G>A