Allele Registry

Canonical Allele Identifier: PA110536

Gene: NOD2 HGNC NCBI

ClinVar RCV:

RCV000416481

ClinVar Variation:

4698

HGVS (amino-acid)	Matching Registered Transcripts
NP_071445.1:p.His496Leu	CA117025 NM_022162.3:c.1487A>T