Allele Registry

Canonical Allele Identifier: PA110545

Gene: NOD2 HGNC NCBI

ClinVar RCV:

RCV000004959

ClinVar Variation:

4695

HGVS (amino-acid)	Matching Registered Transcripts
NP_071445.1:p.Leu469Phe	CA117020 NM_022162.3:c.1405C>T