Canonical Allele Identifier: PA2826835907
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1446312
ClinVar RCV Id: RCV002563461

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.His899Gln
CA395875248
NM_001293557.2:c.2697C>A
CA395875250
NM_001293557.2:c.2697C>G