Allele Registry

Canonical Allele Identifier: PA213416

Gene: NOD2 HGNC NCBI

ClinVar RCV:

RCV000203217

RCV000365422

RCV000416493

RCV001535441

RCV001781186

RCV001810832

RCV002262557

RCV002512783

ClinVar Variation:

4693

HGVS (amino-acid)	Matching Registered Transcripts
NP_071445.1:p.Arg702Trp	CA213414 NM_022162.3:c.2104C>T