Canonical Allele Identifier: PA2826835599
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2934753
ClinVar RCV Id: RCV003798455

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Gly507Asp
CA395869253
NM_001293557.2:c.1520G>A