Canonical Allele Identifier: PA2826835545
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2193820
ClinVar RCV Id: RCV002647250

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Gln447Lys
CA395868882
NM_001293557.2:c.1339C>A