Allele Registry

Canonical Allele Identifier: PA2826835431

Gene: NOD2 HGNC NCBI

ClinVar Allele:

103711

ClinVar RCV:

RCV000084073

RCV001781412

RCV001811395

RCV002513868

ClinVar Variation:

97819

HGVS (amino-acid)	Matching Registered Transcripts
NP_001280486.1:p.Asp330Ala	CA150169 NM_001293557.2:c.989A>C