Allele Registry

Canonical Allele Identifier: PA150171

Gene: NOD2 HGNC NCBI

ClinVar Allele:

103711

ClinVar RCV:

RCV000084073

RCV001781412

RCV001811395

RCV002513868

ClinVar Variation:

97819

HGVS (amino-acid)	Matching Registered Transcripts
NP_071445.1:p.Asp357Ala	CA150169 NM_022162.3:c.1070A>C