Canonical Allele Identifier: PA891850776
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 565494
ClinVar RCV Id: RCV002531432
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Glu498Asp
CA395869044
NM_022162.3:c.1494A>C
CA395869045
NM_022162.3:c.1494A>T