Allele Registry

Canonical Allele Identifier: PA150195

Gene: NOD2 HGNC NCBI

ClinVar RCV:

RCV000084082

RCV000658746

RCV001781415

RCV002513869

ClinVar Variation:

97827

HGVS (amino-acid)	Matching Registered Transcripts
NP_071445.1:p.Glu441Lys	CA150193 NM_022162.3:c.1321G>A