Canonical Allele Identifier: PA2826835752
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 267319
ClinVar RCV Id: RCV000258056
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Val706Leu
CA10590111
NM_001293557.2:c.2116G>T
CA395871303
NM_001293557.2:c.2116G>C