Allele Registry

Canonical Allele Identifier: PA645494203

Gene: NOD2 HGNC NCBI

ClinVar RCV:

RCV000258859

ClinVar Variation:

268134

HGVS (amino-acid)	Matching Registered Transcripts
NP_071445.1:p.Leu349Phe	CA10602671 NM_022162.3:c.1045C>T