Canonical Allele Identifier: PA2826835699
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1499646
ClinVar RCV Id: RCV002642092
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Ala648Val
CA8051675
NM_001293557.2:c.1943C>T