Allele Registry

Canonical Allele Identifier: PA110501

Gene: NOD2 HGNC NCBI

ClinVar RCV:

RCV000084099

RCV000761493

RCV002513874

ClinVar Variation:

97842

623348

HGVS (amino-acid)	Matching Registered Transcripts
NP_071445.1:p.Asn670Lys	CA150239 NM_022162.3:c.2010C>A CA395870549 NM_022162.3:c.2010C>G