Allele Registry

Canonical Allele Identifier: PA1139743002

Gene: NOD2 HGNC NCBI

ClinVar Allele:

949429

ClinVar RCV:

RCV002261314

RCV002563837

ClinVar Variation:

961982

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357395.1:p.Arg982Gly	CA8052049 NM_001370466.1:c.2944A>G