Allele Registry

Canonical Allele Identifier: PA110464

Gene: NOD2 HGNC NCBI

ClinVar RCV:

RCV000328692

RCV001280996

RCV001781188

RCV002512787

RCV003224090

RCV003421904

ClinVar Variation:

4700

HGVS (amino-acid)	Matching Registered Transcripts
NP_071445.1:p.Ala612Thr	CA117029 NM_022162.3:c.1834G>A