Allele Registry

Canonical Allele Identifier: PA645494310

Gene: NOD2 HGNC NCBI

ClinVar Variation Id: 319475

HGVS (amino-acid)	Matching Registered Transcripts
NP_071445.1:p.Gly1032Ser	CA8052076 NM_022162.3:c.3094G>A