Canonical Allele Identifier: PA2828432922
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2934753
ClinVar RCV Id: RCV003798455

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Gly507Asp
CA395869253
NM_001370466.1:c.1520G>A