Canonical Allele Identifier: PA2741976050
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2931636
ClinVar RCV Id: RCV003792658

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Ile251Val
CA281261445
NM_022162.3:c.751A>G