Allele Registry

Canonical Allele Identifier: PA150267

Gene: NOD2 HGNC NCBI

ClinVar RCV:

RCV000084108

RCV000954298

RCV001781421

RCV002260980

RCV002513880

RCV003974995

ClinVar Variation:

97851

HGVS (amino-acid)	Matching Registered Transcripts
NP_071445.1:p.Val793Met	CA150265 NM_022162.3:c.2377G>A