Allele Registry

Canonical Allele Identifier: PA2828432889

Gene: NOD2 HGNC NCBI

ClinVar RCV:

RCV000084089

ClinVar Variation:

97832

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357395.1:p.Cys468Tyr	CA150211 NM_001370466.1:c.1403G>A