Allele Registry

Canonical Allele Identifier: PA2826835568

Gene: NOD2 HGNC NCBI

ClinVar RCV:

RCV002560633

ClinVar Variation:

1429314

HGVS (amino-acid)	Matching Registered Transcripts
NP_001280486.1:p.His469Arg	CA395869027 NM_001293557.2:c.1406A>G