Allele Registry

Canonical Allele Identifier: PA1139746163

Gene: NOD2 HGNC NCBI

ClinVar RCV:

RCV001222153

ClinVar Variation:

950442

HGVS (amino-acid)	Matching Registered Transcripts
NP_071445.1:p.Arg703Gly	CA8051693 NM_022162.3:c.2107C>G