Allele Registry

Canonical Allele Identifier: PA2828433037

Gene: NOD2 HGNC NCBI

ClinVar RCV:

RCV001222153

ClinVar Variation:

950442

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357395.1:p.Arg676Gly	CA8051693 NM_001370466.1:c.2026C>G