Canonical Allele Identifier: PA2828432768
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 838660
ClinVar RCV Id: RCV001040250

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Gly353Asp
CA395868306
NM_001370466.1:c.1058G>A