Canonical Allele Identifier: PA110464
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4700
ClinVar RCV Id: RCV000328692 RCV001280996 RCV001781188 RCV002512787 RCV003421904 RCV003224090
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Ala612Thr
CA117029
NM_022162.3:c.1834G>A