Allele Registry

Canonical Allele Identifier: PA645494181

Gene: NOD2 HGNC NCBI

ClinVar RCV:

RCV000278144

RCV000455970

RCV001782799

RCV001812842

RCV002261057

RCV002521024

ClinVar Variation:

319435

HGVS (amino-acid)	Matching Registered Transcripts
NP_071445.1:p.Pro268Ser	CA8051397 NM_022162.3:c.802C>T