Canonical Allele Identifier: PA1139745566
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 971033
ClinVar RCV Id: RCV002568662

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Val42Leu
CA395865370
NM_022162.3:c.124G>C