Canonical Allele Identifier: PA2741976116
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2939106
ClinVar RCV Id: RCV003791832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Asp399Asn
CA8051491
NM_022162.3:c.1195G>A