Canonical Allele Identifier: PA110554
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97834
ClinVar RCV Id: RCV000084091 RCV002513872
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Met513Thr
CA150217
NM_022162.3:c.1538T>C