Allele Registry

Canonical Allele Identifier: PA645494186

Gene: NOD2 HGNC NCBI

ClinVar RCV:

RCV001121730

RCV001702425

RCV001726112

RCV001782804

RCV002263013

RCV002521029

RCV003972362

ClinVar Variation:

319440

HGVS (amino-acid)	Matching Registered Transcripts
NP_071445.1:p.Asn289Ser	CA8051413 NM_022162.3:c.866A>G