Allele Registry

Canonical Allele Identifier: PA2828433017

Gene: NOD2 HGNC NCBI

ClinVar RCV:

RCV000084099

RCV000761493

RCV002513874

ClinVar Variation:

97842

623348

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357395.1:p.Asn643Lys	CA150239 NM_001370466.1:c.1929C>A CA395870549 NM_001370466.1:c.1929C>G