Allele Registry

Canonical Allele Identifier: PA2826835213

Gene: NOD2 HGNC NCBI

ClinVar Variation Id: 3068617

HGVS (amino-acid)	Matching Registered Transcripts
NP_001280486.1:p.Phe47Leu	CA395865773 NM_001293557.2:c.139T>C CA395865781 NM_001293557.2:c.141C>A CA395865783 NM_001293557.2:c.141C>G