Allele Registry

Canonical Allele Identifier: PA2828432537

Gene: NOD2 HGNC NCBI

ClinVar Allele:

343081

ClinVar RCV:

RCV000322676

RCV001590949

RCV001782788

RCV002522852

ClinVar Variation:

319424

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357395.1:p.Ser20Leu	CA8051207 NM_001370466.1:c.59C>T